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rs794727316

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727316(C;T)
Make rs794727316(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89652870
GeneKIF7
is asnp
is mentioned by
dbSNPrs794727316
ebirs794727316
HLIrs794727316
Exacrs794727316
Varsomers794727316
Maprs794727316
PheGenIrs794727316
hapmaprs794727316
1000 genomesrs794727316
hgdprs794727316
ensemblrs794727316
gopubmedrs794727316
geneviewrs794727316
scholarrs794727316
googlers794727316
pharmgkbrs794727316
gwascentralrs794727316
openSNPrs794727316
23andMers794727316
23andMe allrs794727316
SNP Nexus

SNPshotrs794727316
SNPdbers794727316
MSV3drs794727316
GWAS Ctlgrs794727316
Max Magnitude0
ClinVar
Risk rs794727316(T;T)
Alt rs794727316(T;T)
Reference rs794727316(C;C)
Significance Pathogenic
Disease Acrocallosal syndrome
Variation info
Gene KIF7
CLNDBN Acrocallosal syndrome, Schinzel type
Reversed 1
HGVS NC_000015.9:g.90196101G>A
CLNSRC
CLNACC RCV000176011.1,