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rs775136381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775136381(A;A)
Make rs775136381(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position70976982
GeneFOXP1
is asnp
is mentioned by
dbSNPrs775136381
dbSNP (classic)rs775136381
ClinGenrs775136381
ebirs775136381
HLIrs775136381
Exacrs775136381
Gnomadrs775136381
Varsomers775136381
LitVarrs775136381
Maprs775136381
PheGenIrs775136381
Biobankrs775136381
1000 genomesrs775136381
hgdprs775136381
ensemblrs775136381
geneviewrs775136381
scholarrs775136381
googlers775136381
pharmgkbrs775136381
gwascentralrs775136381
openSNPrs775136381
23andMers775136381
SNPshotrs775136381
SNPdbers775136381
MSV3drs775136381
GWAS Ctlgrs775136381
Max Magnitude0
ClinVar
Risk rs775136381(A;A) rs775136381(C;C) rs775136381(T;T)
Alt rs775136381(A;A) rs775136381(C;C) rs775136381(T;T)
Reference Rs775136381(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXP1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.71026133G>A
CLNSRC
CLNACC RCV000439016.1,