Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503860

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503860(C;T)
Make rs727503860(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60742522
GeneCHD7
is asnp
is mentioned by
dbSNPrs727503860
ebirs727503860
HLIrs727503860
Exacrs727503860
Varsomers727503860
Maprs727503860
PheGenIrs727503860
hapmaprs727503860
1000 genomesrs727503860
hgdprs727503860
ensemblrs727503860
gopubmedrs727503860
geneviewrs727503860
scholarrs727503860
googlers727503860
pharmgkbrs727503860
gwascentralrs727503860
openSNPrs727503860
23andMers727503860
23andMe allrs727503860
SNP Nexus

SNPshotrs727503860
SNPdbers727503860
MSV3drs727503860
GWAS Ctlgrs727503860
Max Magnitude0
ClinVar
Risk rs727503860(T;T)
Alt rs727503860(T;T)
Reference rs727503860(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61655081C>T
CLNSRC
CLNACC RCV000153004.3,