Have questions? Visit https://www.reddit.com/r/SNPedia

rs878852996

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878852996(A;A)
Make rs878852996(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position103316544
GeneDYNC2H1
is asnp
is mentioned by
dbSNPrs878852996
ebirs878852996
HLIrs878852996
Exacrs878852996
Varsomers878852996
Maprs878852996
PheGenIrs878852996
hapmaprs878852996
1000 genomesrs878852996
hgdprs878852996
ensemblrs878852996
gopubmedrs878852996
geneviewrs878852996
scholarrs878852996
googlers878852996
pharmgkbrs878852996
gwascentralrs878852996
openSNPrs878852996
23andMers878852996
23andMe allrs878852996
SNP Nexus

SNPshotrs878852996
SNPdbers878852996
MSV3drs878852996
GWAS Ctlgrs878852996
Max Magnitude0
ClinVar
Risk rs878852996(A;A)
Alt rs878852996(A;A)
Reference rs878852996(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DYNC2H1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.103187273G>A
CLNSRC
CLNACC RCV000224567.1,