Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205143

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205143(A;C)
Make rs786205143(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position154794095
GeneDPP6
is asnp
is mentioned by
dbSNPrs786205143
ebirs786205143
HLIrs786205143
Exacrs786205143
Varsomers786205143
Maprs786205143
PheGenIrs786205143
hapmaprs786205143
1000 genomesrs786205143
hgdprs786205143
ensemblrs786205143
gopubmedrs786205143
geneviewrs786205143
scholarrs786205143
googlers786205143
pharmgkbrs786205143
gwascentralrs786205143
openSNPrs786205143
23andMers786205143
23andMe allrs786205143
SNP Nexus

SNPshotrs786205143
SNPdbers786205143
MSV3drs786205143
GWAS Ctlgrs786205143
Max Magnitude0
ClinVar
Risk rs786205143(C;C)
Alt rs786205143(C;C)
Reference rs786205143(A;A)
Significance Pathogenic
Disease MENTAL RETARDATION
Variation info
Gene DPP6
CLNDBN MENTAL RETARDATION, AUTOSOMAL DOMINANT 33
Reversed 0
HGVS NC_000007.14:g.154794095A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000169782.2,