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Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study
Article first published online: 16 MAR 2012
© 2012 John Wiley & Sons A/S
Pigment Cell & Melanoma Research
Volume 25, Issue 3, pages 384–394, May 2012
How to Cite
Davies, J. R., Randerson-Moor, J., Kukalizch, K., Harland, M., Kumar, R., Madhusudan, S., Nagore, E., Hansson, J., Höiom, V., Ghiorzo, P., Gruis, N. A., Kanetsky, P. A., Wendt, J., Pjanova, D., Puig, S., Saiag, P., Schadendorf, D., Soufir, N., Okamoto, I., Affleck, P., García-Casado, Z., Ogbah, Z., Ozola, A., Queirolo, P., Sucker, A., Barrett, J. H., van Doorn, R., Bishop, D. T. and Newton-Bishop, J. (2012), Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study. Pigment Cell & Melanoma Research, 25: 384–394. doi: 10.1111/j.1755-148X.2012.00982.x
- Issue published online: 17 APR 2012
- Article first published online: 16 MAR 2012
- Accepted manuscript online: 10 FEB 2012 07:16PM EST
- PUBLICATION DATA Received 26 September 2011, revised and accepted for publication 20 January 2012, published online 10 February 2012
Data S1. Methods.
Table S1.MC1R calls including and excluding rare variants determined using the bioinformatic analysis. Variant calls based only on the nine variants described in (Duffy et al. 2004) are in italics, variant calls based upon inclusion of information taken from rare variants are in bold.
Table S2.MC1R status and hair colour in the combined dataset. MC1R is strongly associated with the hair colour phenotype (Pearson’s Chi-squared test <0.0001).
Table S3. MC1R Genotyping method, patient accrual and follow up in each group.
Table S4. Breakdown of the exclusion of cases ineligible for analysis by cohort.
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