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rs879253881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253881(C;T)
Make rs879253881(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position102008244
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879253881
dbSNP (classic)rs879253881
ClinGenrs879253881
ebirs879253881
HLIrs879253881
Exacrs879253881
Gnomadrs879253881
Varsomers879253881
LitVarrs879253881
Maprs879253881
PheGenIrs879253881
Biobankrs879253881
1000 genomesrs879253881
hgdprs879253881
ensemblrs879253881
geneviewrs879253881
scholarrs879253881
googlers879253881
pharmgkbrs879253881
gwascentralrs879253881
openSNPrs879253881
23andMers879253881
SNPshotrs879253881
SNPdbers879253881
MSV3drs879253881
GWAS Ctlgrs879253881
Max Magnitude0
ClinVar
Risk rs879253881(T;T)
Alt rs879253881(T;T)
Reference Rs879253881(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102474581C>T
CLNSRC
CLNACC RCV000236762.1,