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

rs41555013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41555013(A;A)
Make rs41555013(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271066
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41555013
ClinGenrs41555013
ebirs41555013
HLIrs41555013
Exacrs41555013
Varsomers41555013
Maprs41555013
PheGenIrs41555013
hapmaprs41555013
1000 genomesrs41555013
hgdprs41555013
ensemblrs41555013
gopubmedrs41555013
geneviewrs41555013
scholarrs41555013
googlers41555013
pharmgkbrs41555013
gwascentralrs41555013
openSNPrs41555013
23andMers41555013
23andMe allrs41555013
SNP Nexus

SNPshotrs41555013
SNPdbers41555013
MSV3drs41555013
GWAS Ctlgrs41555013
Max Magnitude0
ClinVar
Risk rs41555013(A;A)
Alt rs41555013(A;A)
Reference Rs41555013(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238843C>T
CLNSRC
CLNACC