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rs41544015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41544015(A;A)
Make rs41544015(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271304
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544015
ebirs41544015
HLIrs41544015
Exacrs41544015
Varsomers41544015
Maprs41544015
PheGenIrs41544015
hapmaprs41544015
1000 genomesrs41544015
hgdprs41544015
ensemblrs41544015
gopubmedrs41544015
geneviewrs41544015
scholarrs41544015
googlers41544015
pharmgkbrs41544015
gwascentralrs41544015
openSNPrs41544015
23andMers41544015
23andMe allrs41544015
SNP Nexus

SNPshotrs41544015
SNPdbers41544015
MSV3drs41544015
GWAS Ctlgrs41544015
Max Magnitude0
ClinVar
Risk rs41544015(A,C,T;A,C,T)
Alt rs41544015(A,C,T;A,C,T)
Reference rs41544015(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239081C>A; NC_000006.11:g.31239081C>G; NC_000006.11:g.31239081C>T
CLNSRC
CLNACC