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rs146973734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146973734(C;T)
Make rs146973734(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position7690389
GeneGDF3
is asnp
is mentioned by
dbSNPrs146973734
ebirs146973734
HLIrs146973734
Exacrs146973734
Varsomers146973734
Maprs146973734
PheGenIrs146973734
hapmaprs146973734
1000 genomesrs146973734
hgdprs146973734
ensemblrs146973734
gopubmedrs146973734
geneviewrs146973734
scholarrs146973734
googlers146973734
pharmgkbrs146973734
gwascentralrs146973734
openSNPrs146973734
23andMers146973734
23andMe allrs146973734
SNP Nexus

SNPshotrs146973734
SNPdbers146973734
MSV3drs146973734
GWAS Ctlgrs146973734
Max Magnitude0
ClinVar
Risk rs146973734(T;T)
Alt rs146973734(T;T)
Reference rs146973734(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene GDF3
CLNDBN Microphthalmia, isolated 7
Reversed 0
HGVS NC_000012.11:g.7842985C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023558.2,