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rs41557114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557114(A;A)
Make rs41557114(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271188
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41557114
ebirs41557114
HLIrs41557114
Exacrs41557114
Varsomers41557114
Maprs41557114
PheGenIrs41557114
hapmaprs41557114
1000 genomesrs41557114
hgdprs41557114
ensemblrs41557114
gopubmedrs41557114
geneviewrs41557114
scholarrs41557114
googlers41557114
pharmgkbrs41557114
gwascentralrs41557114
openSNPrs41557114
23andMers41557114
23andMe allrs41557114
SNP Nexus

SNPshotrs41557114
SNPdbers41557114
MSV3drs41557114
GWAS Ctlgrs41557114
Max Magnitude0
ClinVar
Risk rs41557114(A,C,T;A,C,T)
Alt rs41557114(A,C,T;A,C,T)
Reference rs41557114(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238965C>A; NC_000006.11:g.31238965C>G; NC_000006.11:g.31238965C>T
CLNSRC
CLNACC