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rs1060499737

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499737(A;A)
Make rs1060499737(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position124968903
GeneDHX37
is asnp
is mentioned by
dbSNPrs1060499737
dbSNP (old)rs1060499737
ClinGenrs1060499737
ebirs1060499737
HLIrs1060499737
Exacrs1060499737
Gnomadrs1060499737
Varsomers1060499737
Maprs1060499737
PheGenIrs1060499737
Biobankrs1060499737
1000 genomesrs1060499737
hgdprs1060499737
ensemblrs1060499737
gopubmedrs1060499737
geneviewrs1060499737
scholarrs1060499737
googlers1060499737
pharmgkbrs1060499737
gwascentralrs1060499737
openSNPrs1060499737
23andMers1060499737
23andMe allrs1060499737
SNPshotrs1060499737
SNPdbers1060499737
MSV3drs1060499737
GWAS Ctlgrs1060499737
Max Magnitude0
ClinVar
Risk rs1060499737(A;A)
Alt rs1060499737(A;A)
Reference Rs1060499737(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene DHX37
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000012.11:g.125453449G>T
CLNSRC
CLNACC RCV000454218.1,