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rs200172948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200172948(G;T)
Make rs200172948(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271266
GeneHLA-C
is asnp
is mentioned by
dbSNPrs200172948
ebirs200172948
HLIrs200172948
Exacrs200172948
Varsomers200172948
Maprs200172948
PheGenIrs200172948
hapmaprs200172948
1000 genomesrs200172948
hgdprs200172948
ensemblrs200172948
gopubmedrs200172948
geneviewrs200172948
scholarrs200172948
googlers200172948
pharmgkbrs200172948
gwascentralrs200172948
openSNPrs200172948
23andMers200172948
23andMe allrs200172948
SNP Nexus

SNPshotrs200172948
SNPdbers200172948
MSV3drs200172948
GWAS Ctlgrs200172948
Max Magnitude0
ClinVar
Risk rs200172948(A,C,T;A,C,T)
Alt rs200172948(A,C,T;A,C,T)
Reference rs200172948(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239043G>A; NC_000006.11:g.31239043G>C; NC_000006.11:g.31239043G>T
CLNSRC
CLNACC