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rs886041355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position1610901
GeneFOXC1
is asnp
is mentioned by
dbSNPrs886041355
dbSNP (classic)rs886041355
ClinGenrs886041355
ebirs886041355
HLIrs886041355
Exacrs886041355
Gnomadrs886041355
Varsomers886041355
LitVarrs886041355
Maprs886041355
PheGenIrs886041355
Biobankrs886041355
1000 genomesrs886041355
hgdprs886041355
ensemblrs886041355
geneviewrs886041355
scholarrs886041355
googlers886041355
pharmgkbrs886041355
gwascentralrs886041355
openSNPrs886041355
23andMers886041355
23andMe allrs886041355
SNPshotrs886041355
SNPdbers886041355
MSV3drs886041355
GWAS Ctlgrs886041355
Max Magnitude0
ClinVar
Risk rs886041355(A;A)
Alt rs886041355(A;A)
Reference Rs886041355(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1611136G>A
CLNSRC
CLNACC RCV000330423.1,