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

rs41560918

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560918(A;A)
Make rs41560918(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271161
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41560918
ebirs41560918
HLIrs41560918
Exacrs41560918
Varsomers41560918
Maprs41560918
PheGenIrs41560918
hapmaprs41560918
1000 genomesrs41560918
hgdprs41560918
ensemblrs41560918
gopubmedrs41560918
geneviewrs41560918
scholarrs41560918
googlers41560918
pharmgkbrs41560918
gwascentralrs41560918
openSNPrs41560918
23andMers41560918
23andMe allrs41560918
SNP Nexus

SNPshotrs41560918
SNPdbers41560918
MSV3drs41560918
GWAS Ctlgrs41560918
Max Magnitude0
ClinVar
Risk rs41560918(A,C;A,C)
Alt rs41560918(A,C;A,C)
Reference rs41560918(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238938C>G; NC_000006.11:g.31238938C>T
CLNSRC
CLNACC