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rs778139192

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778139192(G;T)
Make rs778139192(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89629561
GeneKIF7
is asnp
is mentioned by
dbSNPrs778139192
ebirs778139192
HLIrs778139192
Exacrs778139192
Varsomers778139192
Maprs778139192
PheGenIrs778139192
hapmaprs778139192
1000 genomesrs778139192
hgdprs778139192
ensemblrs778139192
gopubmedrs778139192
geneviewrs778139192
scholarrs778139192
googlers778139192
pharmgkbrs778139192
gwascentralrs778139192
openSNPrs778139192
23andMers778139192
23andMe allrs778139192
SNP Nexus

SNPshotrs778139192
SNPdbers778139192
MSV3drs778139192
GWAS Ctlgrs778139192
Max Magnitude0
ClinVar
Risk rs778139192(T;T)
Alt rs778139192(T;T)
Reference rs778139192(G;G)
Significance Pathogenic
Disease Acrocallosal syndrome
Variation info
Gene KIF7
CLNDBN Acrocallosal syndrome, Schinzel type
Reversed 0
HGVS NC_000015.9:g.90172792G>A
CLNSRC
CLNACC RCV000201533.1,