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rs1060499772

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499772(C;C)
Make rs1060499772(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position135943412
GeneDARS
is asnp
is mentioned by
dbSNPrs1060499772
dbSNP (old)rs1060499772
ClinGenrs1060499772
ebirs1060499772
HLIrs1060499772
Exacrs1060499772
Gnomadrs1060499772
Varsomers1060499772
LitVarrs1060499772
Maprs1060499772
PheGenIrs1060499772
Biobankrs1060499772
1000 genomesrs1060499772
hgdprs1060499772
ensemblrs1060499772
gopubmedrs1060499772
geneviewrs1060499772
scholarrs1060499772
googlers1060499772
pharmgkbrs1060499772
gwascentralrs1060499772
openSNPrs1060499772
23andMers1060499772
23andMe allrs1060499772
SNPshotrs1060499772
SNPdbers1060499772
MSV3drs1060499772
GWAS Ctlgrs1060499772
Max Magnitude0
ClinVar
Risk rs1060499772(C;C)
Alt rs1060499772(C;C)
Reference Rs1060499772(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene DARS
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000002.11:g.136700982C>G
CLNSRC
CLNACC RCV000454195.1,