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rs185790394

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs185790394(C;G)
Make rs185790394(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position1610202
GeneFOXC1
is asnp
is mentioned by
dbSNPrs185790394
ebirs185790394
HLIrs185790394
Exacrs185790394
Varsomers185790394
Maprs185790394
PheGenIrs185790394
hapmaprs185790394
1000 genomesrs185790394
hgdprs185790394
ensemblrs185790394
gopubmedrs185790394
geneviewrs185790394
scholarrs185790394
googlers185790394
pharmgkbrs185790394
gwascentralrs185790394
openSNPrs185790394
23andMers185790394
23andMe allrs185790394
SNP Nexus

SNPshotrs185790394
SNPdbers185790394
MSV3drs185790394
GWAS Ctlgrs185790394
Max Magnitude0
ClinVar
Risk rs185790394(G,T;G,T)
Alt rs185790394(G,T;G,T)
Reference rs185790394(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1610437C>T
CLNSRC
CLNACC RCV000162083.1,