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rs786200969

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200969(-;-)
Make rs786200969(-;C)
Make rs786200969(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60856183
GeneCHD7
is asnp
is mentioned by
dbSNPrs786200969
ebirs786200969
HLIrs786200969
Exacrs786200969
Varsomers786200969
Maprs786200969
PheGenIrs786200969
hapmaprs786200969
1000 genomesrs786200969
hgdprs786200969
ensemblrs786200969
gopubmedrs786200969
geneviewrs786200969
scholarrs786200969
googlers786200969
pharmgkbrs786200969
gwascentralrs786200969
openSNPrs786200969
23andMers786200969
23andMe allrs786200969
SNP Nexus

SNPshotrs786200969
SNPdbers786200969
MSV3drs786200969
GWAS Ctlgrs786200969
Max Magnitude0
ClinVar
Risk rs786200969(C;C)
Alt rs786200969(C;C)
Reference rs786200969(;)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61768742dupC
CLNSRC
CLNACC RCV000153022.3,