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rs797045535

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045535(A;A)
Make rs797045535(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position102017157
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs797045535
ebirs797045535
HLIrs797045535
Exacrs797045535
Varsomers797045535
Maprs797045535
PheGenIrs797045535
hapmaprs797045535
1000 genomesrs797045535
hgdprs797045535
ensemblrs797045535
gopubmedrs797045535
geneviewrs797045535
scholarrs797045535
googlers797045535
pharmgkbrs797045535
gwascentralrs797045535
openSNPrs797045535
23andMers797045535
23andMe allrs797045535
SNP Nexus

SNPshotrs797045535
SNPdbers797045535
MSV3drs797045535
GWAS Ctlgrs797045535
Max Magnitude0
ClinVar
Risk rs797045535(A;A)
Alt rs797045535(A;A)
Reference rs797045535(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene DYNC1H1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000014.8:g.102483494G>A
CLNSRC
CLNACC RCV000192412.1, RCV000236144.1,