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rs121909355

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909355(A;T)
Make rs121909355(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position96145173
GeneGDF6
is asnp
is mentioned by
dbSNPrs121909355
ebirs121909355
HLIrs121909355
Exacrs121909355
Varsomers121909355
Maprs121909355
PheGenIrs121909355
hapmaprs121909355
1000 genomesrs121909355
hgdprs121909355
ensemblrs121909355
gopubmedrs121909355
geneviewrs121909355
scholarrs121909355
googlers121909355
pharmgkbrs121909355
gwascentralrs121909355
openSNPrs121909355
23andMers121909355
23andMe allrs121909355
SNP Nexus

SNPshotrs121909355
SNPdbers121909355
MSV3drs121909355
GWAS Ctlgrs121909355
Max Magnitude0
OMIM601147
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909355(T;T)
Alt rs121909355(T;T)
Reference rs121909355(A;A)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene GDF6
CLNDBN Microphthalmia, isolated 4
Reversed 1
HGVS NC_000008.10:g.97157401T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008881.2,