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rs137853267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853267(A;G)
Make rs137853267(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position54465797
GeneFGD1
is asnp
is mentioned by
dbSNPrs137853267
ebirs137853267
HLIrs137853267
Exacrs137853267
Varsomers137853267
Maprs137853267
PheGenIrs137853267
hapmaprs137853267
1000 genomesrs137853267
hgdprs137853267
ensemblrs137853267
gopubmedrs137853267
geneviewrs137853267
scholarrs137853267
googlers137853267
pharmgkbrs137853267
gwascentralrs137853267
openSNPrs137853267
23andMers137853267
23andMe allrs137853267
SNP Nexus

SNPshotrs137853267
SNPdbers137853267
MSV3drs137853267
GWAS Ctlgrs137853267
Max Magnitude0
OMIM300546
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137853267(G;G)
Alt rs137853267(G;G)
Reference rs137853267(A;A)
Significance Pathogenic
Disease Aarskog syndrome
Variation info
Gene FGD1
CLNDBN Aarskog syndrome
Reversed 1
HGVS NC_000023.10:g.54492230T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011581.4,