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rs1057518632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518632(G;G)
Make rs1057518632(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position35092535
GenePIGO
is asnp
is mentioned by
dbSNPrs1057518632
dbSNP (classic)rs1057518632
ClinGenrs1057518632
ebirs1057518632
HLIrs1057518632
Exacrs1057518632
Gnomadrs1057518632
Varsomers1057518632
LitVarrs1057518632
Maprs1057518632
PheGenIrs1057518632
Biobankrs1057518632
1000 genomesrs1057518632
hgdprs1057518632
ensemblrs1057518632
geneviewrs1057518632
scholarrs1057518632
googlers1057518632
pharmgkbrs1057518632
gwascentralrs1057518632
openSNPrs1057518632
23andMers1057518632
23andMe allrs1057518632
SNPshotrs1057518632
SNPdbers1057518632
MSV3drs1057518632
GWAS Ctlgrs1057518632
Max Magnitude0
ClinVar
Risk rs1057518632(G;G)
Alt rs1057518632(G;G)
Reference Rs1057518632(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PIGO
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.35092532A>C
CLNSRC
CLNACC RCV000413195.1,