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rs376405759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(T;T) 0 common genotype
Make rs376405759(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position1610691
GeneFOXC1
is asnp
is mentioned by
dbSNPrs376405759
dbSNP (classic)rs376405759
ClinGenrs376405759
ebirs376405759
HLIrs376405759
Exacrs376405759
Gnomadrs376405759
Varsomers376405759
LitVarrs376405759
Maprs376405759
PheGenIrs376405759
Biobankrs376405759
1000 genomesrs376405759
hgdprs376405759
ensemblrs376405759
geneviewrs376405759
scholarrs376405759
googlers376405759
pharmgkbrs376405759
gwascentralrs376405759
openSNPrs376405759
23andMers376405759
23andMe allrs376405759
SNPshotrs376405759
SNPdbers376405759
MSV3drs376405759
GWAS Ctlgrs376405759
Max Magnitude0
ClinVar
Risk rs376405759(G;G) Rs376405759(T;T)
Alt rs376405759(G;G) Rs376405759(T;T)
Reference Rs376405759(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1610926C>G
CLNSRC
CLNACC RCV000255621.1,