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rs41547620

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41547620(A;C)
Make rs41547620(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270484
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41547620
ebirs41547620
HLIrs41547620
Exacrs41547620
Varsomers41547620
Maprs41547620
PheGenIrs41547620
hapmaprs41547620
1000 genomesrs41547620
hgdprs41547620
ensemblrs41547620
gopubmedrs41547620
geneviewrs41547620
scholarrs41547620
googlers41547620
pharmgkbrs41547620
gwascentralrs41547620
openSNPrs41547620
23andMers41547620
23andMe allrs41547620
SNP Nexus

SNPshotrs41547620
SNPdbers41547620
MSV3drs41547620
GWAS Ctlgrs41547620
Max Magnitude0
ClinVar
Risk rs41547620(C;C)
Alt rs41547620(C;C)
Reference rs41547620(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238261T>G
CLNSRC
CLNACC