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rs786201013

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201013(A;T)
Make rs786201013(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position200603922
GeneKIF14
is asnp
is mentioned by
dbSNPrs786201013
ebirs786201013
HLIrs786201013
Exacrs786201013
Varsomers786201013
Maprs786201013
PheGenIrs786201013
hapmaprs786201013
1000 genomesrs786201013
hgdprs786201013
ensemblrs786201013
gopubmedrs786201013
geneviewrs786201013
scholarrs786201013
googlers786201013
pharmgkbrs786201013
gwascentralrs786201013
openSNPrs786201013
23andMers786201013
23andMe allrs786201013
SNP Nexus

SNPshotrs786201013
SNPdbers786201013
MSV3drs786201013
GWAS Ctlgrs786201013
Max Magnitude0
ClinVar
Risk rs786201013(T;T)
Alt rs786201013(T;T)
Reference rs786201013(A;A)
Significance Pathogenic
Disease Meckel syndrome 12
Variation info
Gene KIF14
CLNDBN Meckel syndrome 12
Reversed 1
HGVS NC_000001.10:g.200573050T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162211.3,