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rs1057518999

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518999(C;C)
Make rs1057518999(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position70977826
GeneFOXP1
is asnp
is mentioned by
dbSNPrs1057518999
dbSNP (old)rs1057518999
ClinGenrs1057518999
ebirs1057518999
HLIrs1057518999
Exacrs1057518999
Gnomadrs1057518999
Varsomers1057518999
Maprs1057518999
PheGenIrs1057518999
Biobankrs1057518999
1000 genomesrs1057518999
hgdprs1057518999
ensemblrs1057518999
gopubmedrs1057518999
geneviewrs1057518999
scholarrs1057518999
googlers1057518999
pharmgkbrs1057518999
gwascentralrs1057518999
openSNPrs1057518999
23andMers1057518999
23andMe allrs1057518999
SNPshotrs1057518999
SNPdbers1057518999
MSV3drs1057518999
GWAS Ctlgrs1057518999
Max Magnitude0
ClinVar
Risk rs1057518999(C;C)
Alt rs1057518999(C;C)
Reference Rs1057518999(T;T)
Significance Probable-Pathogenic
Disease Autism
Variation info
Gene FOXP1
CLNDBN Autism
Reversed 1
HGVS NC_000003.11:g.71026977A>G
CLNSRC
CLNACC RCV000414900.1,