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rs1060499736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499736(C;T)
Make rs1060499736(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position129523364
GeneSMARCA1
is asnp
is mentioned by
dbSNPrs1060499736
dbSNP (old)rs1060499736
ClinGenrs1060499736
ebirs1060499736
HLIrs1060499736
Exacrs1060499736
Gnomadrs1060499736
Varsomers1060499736
LitVarrs1060499736
Maprs1060499736
PheGenIrs1060499736
Biobankrs1060499736
1000 genomesrs1060499736
hgdprs1060499736
ensemblrs1060499736
gopubmedrs1060499736
geneviewrs1060499736
scholarrs1060499736
googlers1060499736
pharmgkbrs1060499736
gwascentralrs1060499736
openSNPrs1060499736
23andMers1060499736
23andMe allrs1060499736
SNPshotrs1060499736
SNPdbers1060499736
MSV3drs1060499736
GWAS Ctlgrs1060499736
Max Magnitude0
ClinVar
Risk rs1060499736(T;T)
Alt rs1060499736(T;T)
Reference Rs1060499736(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene SMARCA1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000023.10:g.128657341G>A
CLNSRC
CLNACC RCV000454288.1,