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rs200220845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200220845(C;T)
Make rs200220845(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position60822027
GeneCHD7
is asnp
is mentioned by
dbSNPrs200220845
ebirs200220845
HLIrs200220845
Exacrs200220845
Varsomers200220845
Maprs200220845
PheGenIrs200220845
hapmaprs200220845
1000 genomesrs200220845
hgdprs200220845
ensemblrs200220845
gopubmedrs200220845
geneviewrs200220845
scholarrs200220845
googlers200220845
pharmgkbrs200220845
gwascentralrs200220845
openSNPrs200220845
23andMers200220845
23andMe allrs200220845
SNP Nexus

SNPshotrs200220845
SNPdbers200220845
MSV3drs200220845
GWAS Ctlgrs200220845
Max Magnitude0
ClinVar
Risk rs200220845(A,T;A,T)
Alt rs200220845(A,T;A,T)
Reference rs200220845(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61734586C>T
CLNSRC HGMD
CLNACC RCV000081826.4,