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rs1057523601

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523601(C;T)
Make rs1057523601(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position93020104
GeneCHD2
is asnp
is mentioned by
dbSNPrs1057523601
dbSNP (old)rs1057523601
ClinGenrs1057523601
ebirs1057523601
HLIrs1057523601
Exacrs1057523601
Gnomadrs1057523601
Varsomers1057523601
Maprs1057523601
PheGenIrs1057523601
Biobankrs1057523601
1000 genomesrs1057523601
hgdprs1057523601
ensemblrs1057523601
gopubmedrs1057523601
geneviewrs1057523601
scholarrs1057523601
googlers1057523601
pharmgkbrs1057523601
gwascentralrs1057523601
openSNPrs1057523601
23andMers1057523601
23andMe allrs1057523601
SNPshotrs1057523601
SNPdbers1057523601
MSV3drs1057523601
GWAS Ctlgrs1057523601
Max Magnitude0
ClinVar
Risk rs1057523601(T;T)
Alt rs1057523601(T;T)
Reference Rs1057523601(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93563334C>T
CLNSRC
CLNACC RCV000431354.1,