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rs137853264

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853264(A;A)
Make rs137853264(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position54465522
GeneFGD1
is asnp
is mentioned by
dbSNPrs137853264
ebirs137853264
HLIrs137853264
Exacrs137853264
Varsomers137853264
Maprs137853264
PheGenIrs137853264
hapmaprs137853264
1000 genomesrs137853264
hgdprs137853264
ensemblrs137853264
gopubmedrs137853264
geneviewrs137853264
scholarrs137853264
googlers137853264
pharmgkbrs137853264
gwascentralrs137853264
openSNPrs137853264
23andMers137853264
23andMe allrs137853264
SNP Nexus

SNPshotrs137853264
SNPdbers137853264
MSV3drs137853264
GWAS Ctlgrs137853264
Max Magnitude0
OMIM300546
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853264(A;A)
Alt rs137853264(A;A)
Reference rs137853264(G;G)
Significance Pathogenic
Disease Aarskog syndrome
Variation info
Gene FGD1
CLNDBN Aarskog syndrome
Reversed 1
HGVS NC_000023.10:g.54491955C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011573.2,