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rs3998381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3998381(A;A)
Make rs3998381(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269237
GeneHLA-C
is asnp
is mentioned by
dbSNPrs3998381
ebirs3998381
HLIrs3998381
Exacrs3998381
Varsomers3998381
Maprs3998381
PheGenIrs3998381
hapmaprs3998381
1000 genomesrs3998381
hgdprs3998381
ensemblrs3998381
gopubmedrs3998381
geneviewrs3998381
scholarrs3998381
googlers3998381
pharmgkbrs3998381
gwascentralrs3998381
openSNPrs3998381
23andMers3998381
23andMe allrs3998381
SNP Nexus

SNPshotrs3998381
SNPdbers3998381
MSV3drs3998381
GWAS Ctlgrs3998381
Max Magnitude0
ClinVar
Risk rs3998381(A;A)
Alt rs3998381(A;A)
Reference rs3998381(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237014G>A
CLNSRC
CLNACC