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rs121909356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909356(A;A)
Make rs121909356(A;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position96144951
GeneGDF6
is asnp
is mentioned by
dbSNPrs121909356
ebirs121909356
HLIrs121909356
Exacrs121909356
Varsomers121909356
Maprs121909356
PheGenIrs121909356
hapmaprs121909356
1000 genomesrs121909356
hgdprs121909356
ensemblrs121909356
gopubmedrs121909356
geneviewrs121909356
scholarrs121909356
googlers121909356
pharmgkbrs121909356
gwascentralrs121909356
openSNPrs121909356
23andMers121909356
23andMe allrs121909356
SNP Nexus

SNPshotrs121909356
SNPdbers121909356
MSV3drs121909356
GWAS Ctlgrs121909356
Max Magnitude0
OMIM601147
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909356(A;A)
Alt rs121909356(A;A)
Reference rs121909356(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene GDF6
CLNDBN Microphthalmia, isolated 4
Reversed 1
HGVS NC_000008.10:g.97157179G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008882.3,