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rs104894523

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs104894523(A;A)
Make rs104894523(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position89919733
GeneMC1R
is asnp
is mentioned by
dbSNPrs104894523
ebirs104894523
HLIrs104894523
Exacrs104894523
Varsomers104894523
Maprs104894523
PheGenIrs104894523
hapmaprs104894523
1000 genomesrs104894523
hgdprs104894523
ensemblrs104894523
gopubmedrs104894523
geneviewrs104894523
scholarrs104894523
googlers104894523
pharmgkbrs104894523
gwascentralrs104894523
openSNPrs104894523
23andMers104894523
23andMe allrs104894523
SNP Nexus

SNPshotrs104894523
SNPdbers104894523
MSV3drs104894523
GWAS Ctlgrs104894523
Max Magnitude0
OMIM155555
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894523(A,T;A,T)
Alt rs104894523(A,T;A,T)
Reference rs104894523(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.89986141C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015391.2,