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rs121909501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909501(C;T)
Make rs121909501(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46579986
GeneTDGF1
is asnp
is mentioned by
dbSNPrs121909501
ebirs121909501
HLIrs121909501
Exacrs121909501
Varsomers121909501
Maprs121909501
PheGenIrs121909501
hapmaprs121909501
1000 genomesrs121909501
hgdprs121909501
ensemblrs121909501
gopubmedrs121909501
geneviewrs121909501
scholarrs121909501
googlers121909501
pharmgkbrs121909501
gwascentralrs121909501
openSNPrs121909501
23andMers121909501
23andMe allrs121909501
SNP Nexus

SNPshotrs121909501
SNPdbers121909501
MSV3drs121909501
GWAS Ctlgrs121909501
Max Magnitude0
OMIM187395
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909501(T;T)
Alt rs121909501(T;T)
Reference rs121909501(C;C)
Significance Pathogenic
Disease Forebrain defects
Variation info
Gene LRRC2 TDGF1
CLNDBN Forebrain defects
Reversed 0
HGVS NC_000003.11:g.46621476C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013565.17,