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rs104894524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs104894524(C;T)
Make rs104894524(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89919728
GeneMC1R
is asnp
is mentioned by
dbSNPrs104894524
ebirs104894524
HLIrs104894524
Exacrs104894524
Varsomers104894524
Maprs104894524
PheGenIrs104894524
hapmaprs104894524
1000 genomesrs104894524
hgdprs104894524
ensemblrs104894524
gopubmedrs104894524
geneviewrs104894524
scholarrs104894524
googlers104894524
pharmgkbrs104894524
gwascentralrs104894524
openSNPrs104894524
23andMers104894524
23andMe allrs104894524
SNP Nexus

SNPshotrs104894524
SNPdbers104894524
MSV3drs104894524
GWAS Ctlgrs104894524
Max Magnitude0
OMIM155555
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894524(T;T)
Alt rs104894524(T;T)
Reference Rs104894524(C;C)
Significance Other
Disease Uv-induced skin damage
Variation info
Gene MC1R
CLNDBN Uv-induced skin damage, susceptibility to
Reversed 0
HGVS NC_000016.9:g.89986136C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000015390.2,