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rs794727099

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727099(A;G)
Make rs794727099(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position54450303
GeneFGD1
is asnp
is mentioned by
dbSNPrs794727099
ebirs794727099
HLIrs794727099
Exacrs794727099
Varsomers794727099
Maprs794727099
PheGenIrs794727099
hapmaprs794727099
1000 genomesrs794727099
hgdprs794727099
ensemblrs794727099
gopubmedrs794727099
geneviewrs794727099
scholarrs794727099
googlers794727099
pharmgkbrs794727099
gwascentralrs794727099
openSNPrs794727099
23andMers794727099
23andMe allrs794727099
SNP Nexus

SNPshotrs794727099
SNPdbers794727099
MSV3drs794727099
GWAS Ctlgrs794727099
Max Magnitude0
ClinVar
Risk rs794727099(G;G)
Alt rs794727099(G;G)
Reference rs794727099(A;A)
Significance Pathogenic
Disease Aarskog syndrome
Variation info
Gene FGD1
CLNDBN Aarskog syndrome
Reversed 1
HGVS NC_000023.10:g.54476736T>C
CLNSRC
CLNACC RCV000174537.1,