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rs1057520712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520712(G;T)
Make rs1057520712(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60852900
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057520712
dbSNP (old)rs1057520712
ClinGenrs1057520712
ebirs1057520712
HLIrs1057520712
Exacrs1057520712
Varsomers1057520712
Maprs1057520712
PheGenIrs1057520712
Biobankrs1057520712
1000 genomesrs1057520712
hgdprs1057520712
ensemblrs1057520712
gopubmedrs1057520712
geneviewrs1057520712
scholarrs1057520712
googlers1057520712
pharmgkbrs1057520712
gwascentralrs1057520712
openSNPrs1057520712
23andMers1057520712
23andMe allrs1057520712
SNP Nexus

SNPshotrs1057520712
SNPdbers1057520712
MSV3drs1057520712
GWAS Ctlgrs1057520712
Max Magnitude0
ClinVar
Risk rs1057520712(T;T)
Alt rs1057520712(T;T)
Reference Rs1057520712(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61765459G>T
CLNSRC
CLNACC RCV000438702.1,