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rs879254112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879254112(A;G)
Make rs879254112(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position102002823
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs879254112
dbSNP (classic)rs879254112
ClinGenrs879254112
ebirs879254112
HLIrs879254112
Exacrs879254112
Gnomadrs879254112
Varsomers879254112
LitVarrs879254112
Maprs879254112
PheGenIrs879254112
Biobankrs879254112
1000 genomesrs879254112
hgdprs879254112
ensemblrs879254112
geneviewrs879254112
scholarrs879254112
googlers879254112
pharmgkbrs879254112
gwascentralrs879254112
openSNPrs879254112
23andMers879254112
SNPshotrs879254112
SNPdbers879254112
MSV3drs879254112
GWAS Ctlgrs879254112
Max Magnitude0
ClinVar
Risk rs879254112(G;G)
Alt rs879254112(G;G)
Reference Rs879254112(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYNC1H1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.102469160A>G
CLNSRC
CLNACC RCV000236919.1,