Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909493

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909493(G;T)
Make rs121909493(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position150470162
GeneMAMLD1
is asnp
is mentioned by
dbSNPrs121909493
ebirs121909493
HLIrs121909493
Exacrs121909493
Varsomers121909493
Maprs121909493
PheGenIrs121909493
hapmaprs121909493
1000 genomesrs121909493
hgdprs121909493
ensemblrs121909493
gopubmedrs121909493
geneviewrs121909493
scholarrs121909493
googlers121909493
pharmgkbrs121909493
gwascentralrs121909493
openSNPrs121909493
23andMers121909493
23andMe allrs121909493
SNP Nexus

SNPshotrs121909493
SNPdbers121909493
MSV3drs121909493
GWAS Ctlgrs121909493
Max Magnitude0
OMIM300120
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909493(T;T)
Alt rs121909493(T;T)
Reference rs121909493(G;G)
Significance Pathogenic
Disease Hypospadias 2
Variation info
Gene MAMLD1
CLNDBN Hypospadias 2, X-linked
Reversed 0
HGVS NC_000023.10:g.149638434G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012377.24,