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rs727503861

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503861(C;T)
Make rs727503861(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60742801
GeneCHD7
is asnp
is mentioned by
dbSNPrs727503861
ebirs727503861
HLIrs727503861
Exacrs727503861
Varsomers727503861
Maprs727503861
PheGenIrs727503861
hapmaprs727503861
1000 genomesrs727503861
hgdprs727503861
ensemblrs727503861
gopubmedrs727503861
geneviewrs727503861
scholarrs727503861
googlers727503861
pharmgkbrs727503861
gwascentralrs727503861
openSNPrs727503861
23andMers727503861
23andMe allrs727503861
SNP Nexus

SNPshotrs727503861
SNPdbers727503861
MSV3drs727503861
GWAS Ctlgrs727503861
Max Magnitude0
ClinVar
Risk rs727503861(T;T)
Alt rs727503861(T;T)
Reference rs727503861(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61655360C>T
CLNSRC
CLNACC RCV000153005.3,