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rs1057517956

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517956(G;T)
Make rs1057517956(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60853482
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057517956
dbSNP (old)rs1057517956
ClinGenrs1057517956
ebirs1057517956
HLIrs1057517956
Exacrs1057517956
Gnomadrs1057517956
Varsomers1057517956
Maprs1057517956
PheGenIrs1057517956
Biobankrs1057517956
1000 genomesrs1057517956
hgdprs1057517956
ensemblrs1057517956
gopubmedrs1057517956
geneviewrs1057517956
scholarrs1057517956
googlers1057517956
pharmgkbrs1057517956
gwascentralrs1057517956
openSNPrs1057517956
23andMers1057517956
23andMe allrs1057517956
SNP Nexus

SNPshotrs1057517956
SNPdbers1057517956
MSV3drs1057517956
GWAS Ctlgrs1057517956
Max Magnitude0
ClinVar
Risk rs1057517956(T;T)
Alt rs1057517956(T;T)
Reference Rs1057517956(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61766041G>T
CLNSRC
CLNACC RCV000412832.1,