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rs794727216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727216(A;A)
Make rs794727216(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position70972550
GeneFOXP1
is asnp
is mentioned by
dbSNPrs794727216
dbSNP (classic)rs794727216
ClinGenrs794727216
ebirs794727216
HLIrs794727216
Exacrs794727216
Gnomadrs794727216
Varsomers794727216
LitVarrs794727216
Maprs794727216
PheGenIrs794727216
Biobankrs794727216
1000 genomesrs794727216
hgdprs794727216
ensemblrs794727216
geneviewrs794727216
scholarrs794727216
googlers794727216
pharmgkbrs794727216
gwascentralrs794727216
openSNPrs794727216
23andMers794727216
SNPshotrs794727216
SNPdbers794727216
MSV3drs794727216
GWAS Ctlgrs794727216
Max Magnitude0
ClinVar
Risk rs794727216(A;A)
Alt rs794727216(A;A)
Reference Rs794727216(G;G)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene FOXP1
CLNDBN not specified not provided
Reversed 1
HGVS NC_000003.11:g.71021701C>T
CLNSRC
CLNACC RCV000175371.1, RCV000358706.1,