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rs141007488

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141007488(A;A)
Make rs141007488(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position180986971
GeneDNAJC19
is asnp
is mentioned by
dbSNPrs141007488
ebirs141007488
HLIrs141007488
Exacrs141007488
Varsomers141007488
Maprs141007488
PheGenIrs141007488
hapmaprs141007488
1000 genomesrs141007488
hgdprs141007488
ensemblrs141007488
gopubmedrs141007488
geneviewrs141007488
scholarrs141007488
googlers141007488
pharmgkbrs141007488
gwascentralrs141007488
openSNPrs141007488
23andMers141007488
23andMe allrs141007488
SNP Nexus

SNPshotrs141007488
SNPdbers141007488
MSV3drs141007488
GWAS Ctlgrs141007488
Max Magnitude0
ClinVar
Risk rs141007488(A;A)
Alt rs141007488(A;A)
Reference rs141007488(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNAJC19
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.180704759G>A
CLNSRC
CLNACC RCV000198833.1,