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rs1085307841

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position54446276
GeneFGD1, TSR2
is asnp
is mentioned by
dbSNPrs1085307841
dbSNP (old)rs1085307841
ClinGenrs1085307841
ebirs1085307841
HLIrs1085307841
Exacrs1085307841
Gnomadrs1085307841
Varsomers1085307841
Maprs1085307841
PheGenIrs1085307841
Biobankrs1085307841
1000 genomesrs1085307841
hgdprs1085307841
ensemblrs1085307841
gopubmedrs1085307841
geneviewrs1085307841
scholarrs1085307841
googlers1085307841
pharmgkbrs1085307841
gwascentralrs1085307841
openSNPrs1085307841
23andMers1085307841
23andMe allrs1085307841
SNPshotrs1085307841
SNPdbers1085307841
MSV3drs1085307841
GWAS Ctlgrs1085307841
Max Magnitude0
ClinVar
Risk rs1085307841(T;T)
Alt rs1085307841(T;T)
Reference Rs1085307841(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGD1 TSR2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.54472709C>A
CLNSRC
CLNACC RCV000490039.1,