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rs879253971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253971(G;T)
Make rs879253971(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position102016944
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879253971
dbSNP (classic)rs879253971
ClinGenrs879253971
ebirs879253971
HLIrs879253971
Exacrs879253971
Gnomadrs879253971
Varsomers879253971
LitVarrs879253971
Maprs879253971
PheGenIrs879253971
Biobankrs879253971
1000 genomesrs879253971
hgdprs879253971
ensemblrs879253971
geneviewrs879253971
scholarrs879253971
googlers879253971
pharmgkbrs879253971
gwascentralrs879253971
openSNPrs879253971
23andMers879253971
SNPshotrs879253971
SNPdbers879253971
MSV3drs879253971
GWAS Ctlgrs879253971
Max Magnitude0
ClinVar
Risk rs879253971(T;T)
Alt rs879253971(T;T)
Reference Rs879253971(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102483281G>T
CLNSRC
CLNACC RCV000235681.1,