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rs1085307508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome6
Position1610699
GeneFOXC1
is asnp
is mentioned by
dbSNPrs1085307508
dbSNP (classic)rs1085307508
ClinGenrs1085307508
ebirs1085307508
HLIrs1085307508
Exacrs1085307508
Gnomadrs1085307508
Varsomers1085307508
LitVarrs1085307508
Maprs1085307508
PheGenIrs1085307508
Biobankrs1085307508
1000 genomesrs1085307508
hgdprs1085307508
ensemblrs1085307508
geneviewrs1085307508
scholarrs1085307508
googlers1085307508
pharmgkbrs1085307508
gwascentralrs1085307508
openSNPrs1085307508
23andMers1085307508
23andMe allrs1085307508
SNPshotrs1085307508
SNPdbers1085307508
MSV3drs1085307508
GWAS Ctlgrs1085307508
Max Magnitude0
ClinVar
Risk rs1085307508(T;T)
Alt rs1085307508(T;T)
Reference Rs1085307508(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1610934C>T
CLNSRC
CLNACC RCV000490231.1,