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rs1057518926

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518926(C;G)
Make rs1057518926(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position70977675
GeneFOXP1
is asnp
is mentioned by
dbSNPrs1057518926
dbSNP (old)rs1057518926
ClinGenrs1057518926
ebirs1057518926
HLIrs1057518926
Exacrs1057518926
Gnomadrs1057518926
Varsomers1057518926
Maprs1057518926
PheGenIrs1057518926
Biobankrs1057518926
1000 genomesrs1057518926
hgdprs1057518926
ensemblrs1057518926
gopubmedrs1057518926
geneviewrs1057518926
scholarrs1057518926
googlers1057518926
pharmgkbrs1057518926
gwascentralrs1057518926
openSNPrs1057518926
23andMers1057518926
23andMe allrs1057518926
SNPshotrs1057518926
SNPdbers1057518926
MSV3drs1057518926
GWAS Ctlgrs1057518926
Max Magnitude0
ClinVar
Risk rs1057518926(G;G)
Alt rs1057518926(G;G)
Reference Rs1057518926(C;C)
Significance Probable-Pathogenic
Disease Anterior creases of earlobe Delayed speech and language development Glabellar hemangioma Intellectual disability Strabismus
Variation info
Gene FOXP1
CLNDBN Anterior creases of earlobe Delayed speech and language development Glabellar hemangioma Intellectual disability Strabismus
Reversed 1
HGVS NC_000003.11:g.71026826G>C
CLNSRC
CLNACC RCV000414948.1,