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

rs41555616

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555616(C;G)
Make rs41555616(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271082
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41555616
ebirs41555616
HLIrs41555616
Exacrs41555616
Varsomers41555616
Maprs41555616
PheGenIrs41555616
hapmaprs41555616
1000 genomesrs41555616
hgdprs41555616
ensemblrs41555616
gopubmedrs41555616
geneviewrs41555616
scholarrs41555616
googlers41555616
pharmgkbrs41555616
gwascentralrs41555616
openSNPrs41555616
23andMers41555616
23andMe allrs41555616
SNP Nexus

SNPshotrs41555616
SNPdbers41555616
MSV3drs41555616
GWAS Ctlgrs41555616
Max Magnitude0
ClinVar
Risk rs41555616(G;G)
Alt rs41555616(G;G)
Reference rs41555616(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238859G>C
CLNSRC
CLNACC