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rs1085307886

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome4
Position125468697
GeneFAT4
is asnp
is mentioned by
dbSNPrs1085307886
dbSNP (old)rs1085307886
ClinGenrs1085307886
ebirs1085307886
HLIrs1085307886
Exacrs1085307886
Gnomadrs1085307886
Varsomers1085307886
Maprs1085307886
PheGenIrs1085307886
Biobankrs1085307886
1000 genomesrs1085307886
hgdprs1085307886
ensemblrs1085307886
gopubmedrs1085307886
geneviewrs1085307886
scholarrs1085307886
googlers1085307886
pharmgkbrs1085307886
gwascentralrs1085307886
openSNPrs1085307886
23andMers1085307886
23andMe allrs1085307886
SNPshotrs1085307886
SNPdbers1085307886
MSV3drs1085307886
GWAS Ctlgrs1085307886
Max Magnitude0
ClinVar
Risk rs1085307886(A;A)
Alt rs1085307886(A;A)
Reference Rs1085307886(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FAT4
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.126389852G>A
CLNSRC
CLNACC RCV000489558.1,