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rs17413678

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17413678(C;C)
Make rs17413678(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271089
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17413678
ebirs17413678
HLIrs17413678
Exacrs17413678
Varsomers17413678
Maprs17413678
PheGenIrs17413678
hapmaprs17413678
1000 genomesrs17413678
hgdprs17413678
ensemblrs17413678
gopubmedrs17413678
geneviewrs17413678
scholarrs17413678
googlers17413678
pharmgkbrs17413678
gwascentralrs17413678
openSNPrs17413678
23andMers17413678
23andMe allrs17413678
SNP Nexus

SNPshotrs17413678
SNPdbers17413678
MSV3drs17413678
GWAS Ctlgrs17413678
Max Magnitude0
ClinVar
Risk rs17413678(A,C;A,C)
Alt rs17413678(A,C;A,C)
Reference rs17413678(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238866C>G; NC_000006.11:g.31238866C>T
CLNSRC
CLNACC