Have questions? Visit https://www.reddit.com/r/SNPedia

rs201441823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201441823(C;C)
Make rs201441823(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271335
GeneHLA-C
is asnp
is mentioned by
dbSNPrs201441823
ebirs201441823
HLIrs201441823
Exacrs201441823
Varsomers201441823
Maprs201441823
PheGenIrs201441823
hapmaprs201441823
1000 genomesrs201441823
hgdprs201441823
ensemblrs201441823
gopubmedrs201441823
geneviewrs201441823
scholarrs201441823
googlers201441823
pharmgkbrs201441823
gwascentralrs201441823
openSNPrs201441823
23andMers201441823
23andMe allrs201441823
SNP Nexus

SNPshotrs201441823
SNPdbers201441823
MSV3drs201441823
GWAS Ctlgrs201441823
Max Magnitude0
ClinVar
Risk rs201441823(A,C,T;A,C,T)
Alt rs201441823(A,C,T;A,C,T)
Reference rs201441823(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene HLA-C
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000006.12:g.31271335G>C
CLNSRC ClinVar
CLNACC RCV000067280.2,