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rs1057524501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524501(A;T)
Make rs1057524501(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60841719
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057524501
dbSNP (old)rs1057524501
ClinGenrs1057524501
ebirs1057524501
HLIrs1057524501
Exacrs1057524501
Varsomers1057524501
Maprs1057524501
PheGenIrs1057524501
Biobankrs1057524501
1000 genomesrs1057524501
hgdprs1057524501
ensemblrs1057524501
gopubmedrs1057524501
geneviewrs1057524501
scholarrs1057524501
googlers1057524501
pharmgkbrs1057524501
gwascentralrs1057524501
openSNPrs1057524501
23andMers1057524501
23andMe allrs1057524501
SNP Nexus

SNPshotrs1057524501
SNPdbers1057524501
MSV3drs1057524501
GWAS Ctlgrs1057524501
Max Magnitude0
ClinVar
Risk rs1057524501(T;T)
Alt rs1057524501(T;T)
Reference Rs1057524501(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61754278A>T
CLNSRC
CLNACC RCV000423451.1,