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rs1057518128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518128(C;T)
Make rs1057518128(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position92927289
GeneCHD2
is asnp
is mentioned by
dbSNPrs1057518128
dbSNP (old)rs1057518128
ClinGenrs1057518128
ebirs1057518128
HLIrs1057518128
Exacrs1057518128
Gnomadrs1057518128
Varsomers1057518128
Maprs1057518128
PheGenIrs1057518128
Biobankrs1057518128
1000 genomesrs1057518128
hgdprs1057518128
ensemblrs1057518128
gopubmedrs1057518128
geneviewrs1057518128
scholarrs1057518128
googlers1057518128
pharmgkbrs1057518128
gwascentralrs1057518128
openSNPrs1057518128
23andMers1057518128
23andMe allrs1057518128
SNPshotrs1057518128
SNPdbers1057518128
MSV3drs1057518128
GWAS Ctlgrs1057518128
Max Magnitude0
ClinVar
Risk rs1057518128(T;T)
Alt rs1057518128(T;T)
Reference Rs1057518128(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93470519C>T
CLNSRC
CLNACC RCV000413171.1,