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

rs398124162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124162(-;-)
Make rs398124162(-;C)
Make rs398124162(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position54449671
GeneFGD1
is asnp
is mentioned by
dbSNPrs398124162
ebirs398124162
HLIrs398124162
Exacrs398124162
Varsomers398124162
Maprs398124162
PheGenIrs398124162
hapmaprs398124162
1000 genomesrs398124162
hgdprs398124162
ensemblrs398124162
gopubmedrs398124162
geneviewrs398124162
scholarrs398124162
googlers398124162
pharmgkbrs398124162
gwascentralrs398124162
openSNPrs398124162
23andMers398124162
23andMe allrs398124162
SNP Nexus

SNPshotrs398124162
SNPdbers398124162
MSV3drs398124162
GWAS Ctlgrs398124162
Max Magnitude0
ClinVar
Risk rs398124162(C;C)
Alt rs398124162(C;C)
Reference rs398124162(;)
Significance Pathogenic
Disease not provided Aarskog syndrome
Variation info
Gene FGD1
CLNDBN not provided Aarskog syndrome
Reversed 1
HGVS NC_000023.10:g.54476105dupG
CLNSRC ClinVar
CLNACC RCV000081093.3, RCV000174748.1,