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

rs41557216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557216(A;A)
Make rs41557216(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271230
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41557216
dbSNP (classic)rs41557216
ClinGenrs41557216
ebirs41557216
HLIrs41557216
Exacrs41557216
Gnomadrs41557216
Varsomers41557216
LitVarrs41557216
Maprs41557216
PheGenIrs41557216
Biobankrs41557216
1000 genomesrs41557216
hgdprs41557216
ensemblrs41557216
geneviewrs41557216
scholarrs41557216
googlers41557216
pharmgkbrs41557216
gwascentralrs41557216
openSNPrs41557216
23andMers41557216
SNPshotrs41557216
SNPdbers41557216
MSV3drs41557216
GWAS Ctlgrs41557216
Max Magnitude0
ClinVar
Risk rs41557216(A;A)
Alt rs41557216(A;A)
Reference Rs41557216(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239007C>T
CLNSRC
CLNACC