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rs750047137

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750047137(A;A)
Make rs750047137(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60853254
GeneCHD7
is asnp
is mentioned by
dbSNPrs750047137
ebirs750047137
HLIrs750047137
Exacrs750047137
Varsomers750047137
Maprs750047137
PheGenIrs750047137
hapmaprs750047137
1000 genomesrs750047137
hgdprs750047137
ensemblrs750047137
gopubmedrs750047137
geneviewrs750047137
scholarrs750047137
googlers750047137
pharmgkbrs750047137
gwascentralrs750047137
openSNPrs750047137
23andMers750047137
23andMe allrs750047137
SNP Nexus

SNPshotrs750047137
SNPdbers750047137
MSV3drs750047137
GWAS Ctlgrs750047137
Max Magnitude0
ClinVar
Risk rs750047137(A;A)
Alt rs750047137(A;A)
Reference rs750047137(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61765813G>T
CLNSRC
CLNACC RCV000177569.1,