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rs878852999

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878852999(A;A)
Make rs878852999(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position180988230
GeneDNAJC19
is asnp
is mentioned by
dbSNPrs878852999
ebirs878852999
HLIrs878852999
Exacrs878852999
Varsomers878852999
Maprs878852999
PheGenIrs878852999
hapmaprs878852999
1000 genomesrs878852999
hgdprs878852999
ensemblrs878852999
gopubmedrs878852999
geneviewrs878852999
scholarrs878852999
googlers878852999
pharmgkbrs878852999
gwascentralrs878852999
openSNPrs878852999
23andMers878852999
23andMe allrs878852999
SNP Nexus

SNPshotrs878852999
SNPdbers878852999
MSV3drs878852999
GWAS Ctlgrs878852999
Max Magnitude0
ClinVar
Risk rs878852999(A;A)
Alt rs878852999(A;A)
Reference rs878852999(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNAJC19
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.180706018C>T
CLNSRC
CLNACC RCV000224106.1,