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rs72558149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558149(A;A)
Make rs72558149(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270259
GeneHLA-C
is asnp
is mentioned by
dbSNPrs72558149
dbSNP (classic)rs72558149
ClinGenrs72558149
ebirs72558149
HLIrs72558149
Exacrs72558149
Gnomadrs72558149
Varsomers72558149
LitVarrs72558149
Maprs72558149
PheGenIrs72558149
Biobankrs72558149
1000 genomesrs72558149
hgdprs72558149
ensemblrs72558149
geneviewrs72558149
scholarrs72558149
googlers72558149
pharmgkbrs72558149
gwascentralrs72558149
openSNPrs72558149
23andMers72558149
SNPshotrs72558149
SNPdbers72558149
MSV3drs72558149
GWAS Ctlgrs72558149
Max Magnitude0
ClinVar
Risk rs72558149(A;A) rs72558149(C;C)
Alt rs72558149(A;A) rs72558149(C;C)
Reference Rs72558149(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238036C>G; NC_000006.11:g.31238036C>T
CLNSRC
CLNACC