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rs879254085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879254085(G;T)
Make rs879254085(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position101986018
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879254085
dbSNP (classic)rs879254085
ClinGenrs879254085
ebirs879254085
HLIrs879254085
Exacrs879254085
Gnomadrs879254085
Varsomers879254085
LitVarrs879254085
Maprs879254085
PheGenIrs879254085
Biobankrs879254085
1000 genomesrs879254085
hgdprs879254085
ensemblrs879254085
geneviewrs879254085
scholarrs879254085
googlers879254085
pharmgkbrs879254085
gwascentralrs879254085
openSNPrs879254085
23andMers879254085
SNPshotrs879254085
SNPdbers879254085
MSV3drs879254085
GWAS Ctlgrs879254085
Max Magnitude0
ClinVar
Risk rs879254085(T;T)
Alt rs879254085(T;T)
Reference Rs879254085(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102452355G>A; NC_000014.8:g.102452355G>T
CLNSRC
CLNACC RCV000493258.1, RCV000235287.1,