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rs1064794248

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60838229
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064794248
dbSNP (classic)rs1064794248
ClinGenrs1064794248
ebirs1064794248
HLIrs1064794248
Exacrs1064794248
Gnomadrs1064794248
Varsomers1064794248
LitVarrs1064794248
Maprs1064794248
PheGenIrs1064794248
Biobankrs1064794248
1000 genomesrs1064794248
hgdprs1064794248
ensemblrs1064794248
geneviewrs1064794248
scholarrs1064794248
googlers1064794248
pharmgkbrs1064794248
gwascentralrs1064794248
openSNPrs1064794248
23andMers1064794248
23andMe allrs1064794248
SNPshotrs1064794248
SNPdbers1064794248
MSV3drs1064794248
GWAS Ctlgrs1064794248
Max Magnitude0
ClinVar
Risk rs1064794248(T;T)
Alt rs1064794248(T;T)
Reference Rs1064794248(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61750788G>T
CLNSRC
CLNACC RCV000485855.1,