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rs752274637

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752274637(A;A)
Make rs752274637(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position35737405
GeneCREB3, GBA2
is asnp
is mentioned by
dbSNPrs752274637
ebirs752274637
HLIrs752274637
Exacrs752274637
Varsomers752274637
Maprs752274637
PheGenIrs752274637
hapmaprs752274637
1000 genomesrs752274637
hgdprs752274637
ensemblrs752274637
gopubmedrs752274637
geneviewrs752274637
scholarrs752274637
googlers752274637
pharmgkbrs752274637
gwascentralrs752274637
openSNPrs752274637
23andMers752274637
23andMe allrs752274637
SNP Nexus

SNPshotrs752274637
SNPdbers752274637
MSV3drs752274637
GWAS Ctlgrs752274637
Max Magnitude0
ClinVar
Risk rs752274637(A;A)
Alt rs752274637(A;A)
Reference rs752274637(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CREB3 GBA2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.35737402G>A
CLNSRC
CLNACC RCV000171423.1,