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rs398124156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124156(C;T)
Make rs398124156(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position54465725
GeneFGD1
is asnp
is mentioned by
dbSNPrs398124156
ebirs398124156
HLIrs398124156
Exacrs398124156
Varsomers398124156
Maprs398124156
PheGenIrs398124156
hapmaprs398124156
1000 genomesrs398124156
hgdprs398124156
ensemblrs398124156
gopubmedrs398124156
geneviewrs398124156
scholarrs398124156
googlers398124156
pharmgkbrs398124156
gwascentralrs398124156
openSNPrs398124156
23andMers398124156
23andMe allrs398124156
SNP Nexus

SNPshotrs398124156
SNPdbers398124156
MSV3drs398124156
GWAS Ctlgrs398124156
Max Magnitude0
ClinVar
Risk rs398124156(T;T)
Alt rs398124156(T;T)
Reference rs398124156(C;C)
Significance Pathogenic
Disease not provided Aarskog syndrome
Variation info
Gene FGD1
CLNDBN not provided Aarskog syndrome
Reversed 1
HGVS NC_000023.10:g.54492158G>A
CLNSRC ClinVar Emory University
CLNACC RCV000081085.3, RCV000179887.1,