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rs483352810

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483352810(G;G)
Make rs483352810(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position1610822
GeneFOXC1
is asnp
is mentioned by
dbSNPrs483352810
ebirs483352810
HLIrs483352810
Exacrs483352810
Varsomers483352810
Maprs483352810
PheGenIrs483352810
hapmaprs483352810
1000 genomesrs483352810
hgdprs483352810
ensemblrs483352810
gopubmedrs483352810
geneviewrs483352810
scholarrs483352810
googlers483352810
pharmgkbrs483352810
gwascentralrs483352810
openSNPrs483352810
23andMers483352810
23andMe allrs483352810
SNP Nexus

SNPshotrs483352810
SNPdbers483352810
MSV3drs483352810
GWAS Ctlgrs483352810
Max Magnitude0
ClinVar
Risk rs483352810(G;G)
Alt rs483352810(G;G)
Reference rs483352810(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1611057T>G
CLNSRC
CLNACC RCV000190253.1,