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rs879255410

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255410(-;-)
Make rs879255410(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position60836258
GeneCHD7
is asnp
is mentioned by
dbSNPrs879255410
ebirs879255410
HLIrs879255410
Exacrs879255410
Varsomers879255410
Maprs879255410
PheGenIrs879255410
hapmaprs879255410
1000 genomesrs879255410
hgdprs879255410
ensemblrs879255410
gopubmedrs879255410
geneviewrs879255410
scholarrs879255410
googlers879255410
pharmgkbrs879255410
gwascentralrs879255410
openSNPrs879255410
23andMers879255410
23andMe allrs879255410
SNP Nexus

SNPshotrs879255410
SNPdbers879255410
MSV3drs879255410
GWAS Ctlgrs879255410
Max Magnitude0
ClinVar
Risk rs879255410(;)
Alt rs879255410(;)
Reference rs879255410(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61748817delC
CLNSRC
CLNACC RCV000238786.1,