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rs372857241

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372857241(C;T)
Make rs372857241(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position1610586
GeneFOXC1
is asnp
is mentioned by
dbSNPrs372857241
ebirs372857241
HLIrs372857241
Exacrs372857241
Varsomers372857241
Maprs372857241
PheGenIrs372857241
hapmaprs372857241
1000 genomesrs372857241
hgdprs372857241
ensemblrs372857241
gopubmedrs372857241
geneviewrs372857241
scholarrs372857241
googlers372857241
pharmgkbrs372857241
gwascentralrs372857241
openSNPrs372857241
23andMers372857241
23andMe allrs372857241
SNP Nexus

SNPshotrs372857241
SNPdbers372857241
MSV3drs372857241
GWAS Ctlgrs372857241
Max Magnitude0
ClinVar
Risk rs372857241(G,T;G,T)
Alt rs372857241(G,T;G,T)
Reference rs372857241(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1610821C>G
CLNSRC
CLNACC RCV000190252.1,