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rs398124155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124155(G;G)
Make rs398124155(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position54467837
GeneFGD1
is asnp
is mentioned by
dbSNPrs398124155
ebirs398124155
HLIrs398124155
Exacrs398124155
Varsomers398124155
Maprs398124155
PheGenIrs398124155
hapmaprs398124155
1000 genomesrs398124155
hgdprs398124155
ensemblrs398124155
gopubmedrs398124155
geneviewrs398124155
scholarrs398124155
googlers398124155
pharmgkbrs398124155
gwascentralrs398124155
openSNPrs398124155
23andMers398124155
23andMe allrs398124155
SNP Nexus

SNPshotrs398124155
SNPdbers398124155
MSV3drs398124155
GWAS Ctlgrs398124155
Max Magnitude0
ClinVar
Risk rs398124155(G;G)
Alt rs398124155(G;G)
Reference rs398124155(T;T)
Significance Pathogenic
Disease not provided Aarskog syndrome
Variation info
Gene FGD1
CLNDBN not provided Aarskog syndrome
Reversed 1
HGVS NC_000023.10:g.54494270A>C
CLNSRC ClinVar Emory University
CLNACC RCV000081084.3, RCV000179441.1,