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rs41547622

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41547622(C;C)
Make rs41547622(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270348
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41547622
ebirs41547622
HLIrs41547622
Exacrs41547622
Varsomers41547622
Maprs41547622
PheGenIrs41547622
hapmaprs41547622
1000 genomesrs41547622
hgdprs41547622
ensemblrs41547622
gopubmedrs41547622
geneviewrs41547622
scholarrs41547622
googlers41547622
pharmgkbrs41547622
gwascentralrs41547622
openSNPrs41547622
23andMers41547622
23andMe allrs41547622
SNP Nexus

SNPshotrs41547622
SNPdbers41547622
MSV3drs41547622
GWAS Ctlgrs41547622
Max Magnitude0
ClinVar
Risk rs41547622(C;C)
Alt rs41547622(C;C)
Reference rs41547622(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238125C>G
CLNSRC
CLNACC