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rs114343571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs114343571(A;A)
Make rs114343571(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270788
GeneHLA-C
is asnp
is mentioned by
dbSNPrs114343571
ebirs114343571
HLIrs114343571
Exacrs114343571
Varsomers114343571
Maprs114343571
PheGenIrs114343571
hapmaprs114343571
1000 genomesrs114343571
hgdprs114343571
ensemblrs114343571
gopubmedrs114343571
geneviewrs114343571
scholarrs114343571
googlers114343571
pharmgkbrs114343571
gwascentralrs114343571
openSNPrs114343571
23andMers114343571
23andMe allrs114343571
SNP Nexus

SNPshotrs114343571
SNPdbers114343571
MSV3drs114343571
GWAS Ctlgrs114343571
Max Magnitude0
ClinVar
Risk rs114343571(A;A)
Alt rs114343571(A;A)
Reference rs114343571(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238565G>A
CLNSRC
CLNACC