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rs3188996

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common in complete genomics
Make rs3188996(C;C)
Make rs3188996(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position113235496
GeneC15orf34, PAX8
is asnp
is mentioned by
dbSNPrs3188996
ebirs3188996
HLIrs3188996
Exacrs3188996
Varsomers3188996
Maprs3188996
PheGenIrs3188996
hapmaprs3188996
1000 genomesrs3188996
hgdprs3188996
ensemblrs3188996
gopubmedrs3188996
geneviewrs3188996
scholarrs3188996
googlers3188996
pharmgkbrs3188996
gwascentralrs3188996
openSNPrs3188996
23andMers3188996
23andMe allrs3188996
SNP Nexus

SNPshotrs3188996
SNPdbers3188996
MSV3drs3188996
GWAS Ctlgrs3188996
GMAF0.006428
Max Magnitude0
OMIM167415
DescPAX8 POLYMORPHISM
Variant0001
Relatedalso


ClinVar
Risk rs3188996(C;C)
Alt rs3188996(C;C)
Reference rs3188996(T;T)
Significance Non-pathogenic
Disease PAX8 POLYMORPHISM
Variation info
Gene PAX8 PAX8-AS1
CLNDBN PAX8 POLYMORPHISM
Reversed 1
HGVS NC_000002.11:g.113993073A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014792.3,