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rs786205660

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205660(-;-)
Make rs786205660(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position120568376
GeneCDK5RAP2
is asnp
is mentioned by
dbSNPrs786205660
ebirs786205660
HLIrs786205660
Exacrs786205660
Varsomers786205660
Maprs786205660
PheGenIrs786205660
hapmaprs786205660
1000 genomesrs786205660
hgdprs786205660
ensemblrs786205660
gopubmedrs786205660
geneviewrs786205660
scholarrs786205660
googlers786205660
pharmgkbrs786205660
gwascentralrs786205660
openSNPrs786205660
23andMers786205660
23andMe allrs786205660
SNP Nexus

SNPshotrs786205660
SNPdbers786205660
MSV3drs786205660
GWAS Ctlgrs786205660
Max Magnitude0
ClinVar
Risk rs786205660(;)
Alt rs786205660(;)
Reference rs786205660(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDK5RAP2
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.123330654delA
CLNSRC
CLNACC RCV000171539.1,