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rs74500356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74500356(A;A)
Make rs74500356(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270417
GeneHLA-C
is asnp
is mentioned by
dbSNPrs74500356
ebirs74500356
HLIrs74500356
Exacrs74500356
Varsomers74500356
Maprs74500356
PheGenIrs74500356
hapmaprs74500356
1000 genomesrs74500356
hgdprs74500356
ensemblrs74500356
gopubmedrs74500356
geneviewrs74500356
scholarrs74500356
googlers74500356
pharmgkbrs74500356
gwascentralrs74500356
openSNPrs74500356
23andMers74500356
23andMe allrs74500356
SNP Nexus

SNPshotrs74500356
SNPdbers74500356
MSV3drs74500356
GWAS Ctlgrs74500356
Max Magnitude0
ClinVar
Risk rs74500356(A;A)
Alt rs74500356(A;A)
Reference rs74500356(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238194G>T
CLNSRC
CLNACC