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rs1060499743

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499743(G;G)
Make rs1060499743(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position24596030
GeneARHGAP21
is asnp
is mentioned by
dbSNPrs1060499743
dbSNP (old)rs1060499743
ClinGenrs1060499743
ebirs1060499743
HLIrs1060499743
Exacrs1060499743
Gnomadrs1060499743
Varsomers1060499743
Maprs1060499743
PheGenIrs1060499743
Biobankrs1060499743
1000 genomesrs1060499743
hgdprs1060499743
ensemblrs1060499743
gopubmedrs1060499743
geneviewrs1060499743
scholarrs1060499743
googlers1060499743
pharmgkbrs1060499743
gwascentralrs1060499743
openSNPrs1060499743
23andMers1060499743
23andMe allrs1060499743
SNPshotrs1060499743
SNPdbers1060499743
MSV3drs1060499743
GWAS Ctlgrs1060499743
Max Magnitude0
ClinVar
Risk rs1060499743(G;G)
Alt rs1060499743(G;G)
Reference Rs1060499743(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ARHGAP21
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000010.10:g.24884959A>C
CLNSRC
CLNACC RCV000454179.1,