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rs786205164

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205164(A;A)
Make rs786205164(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position151055276
GeneCDK5
is asnp
is mentioned by
dbSNPrs786205164
ebirs786205164
HLIrs786205164
Exacrs786205164
Varsomers786205164
Maprs786205164
PheGenIrs786205164
hapmaprs786205164
1000 genomesrs786205164
hgdprs786205164
ensemblrs786205164
gopubmedrs786205164
geneviewrs786205164
scholarrs786205164
googlers786205164
pharmgkbrs786205164
gwascentralrs786205164
openSNPrs786205164
23andMers786205164
23andMe allrs786205164
SNP Nexus

SNPshotrs786205164
SNPdbers786205164
MSV3drs786205164
GWAS Ctlgrs786205164
Max Magnitude0
ClinVar
Risk rs786205164(A;A)
Alt rs786205164(A;A)
Reference rs786205164(G;G)
Significance Pathogenic
Disease Lissencephaly 7 with cerebellar hypoplasia
Variation info
Gene CDK5
CLNDBN Lissencephaly 7 with cerebellar hypoplasia
Reversed 1
HGVS NC_000007.13:g.150752363C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170351.4,