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rs17408553

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17408553(A;A)
Make rs17408553(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271630
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17408553
ebirs17408553
HLIrs17408553
Exacrs17408553
Varsomers17408553
Maprs17408553
PheGenIrs17408553
hapmaprs17408553
1000 genomesrs17408553
hgdprs17408553
ensemblrs17408553
gopubmedrs17408553
geneviewrs17408553
scholarrs17408553
googlers17408553
pharmgkbrs17408553
gwascentralrs17408553
openSNPrs17408553
23andMers17408553
23andMe allrs17408553
SNP Nexus

SNPshotrs17408553
SNPdbers17408553
MSV3drs17408553
GWAS Ctlgrs17408553
GMAF0.3632
Max Magnitude0
ClinVar
Risk rs17408553(A,T;A,T)
Alt rs17408553(A,T;A,T)
Reference rs17408553(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239407G>A; NC_000006.11:g.31239407G>T
CLNSRC
CLNACC