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rs761573352

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761573352(A;A)
Make rs761573352(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89101270
GeneACSF3
is asnp
is mentioned by
dbSNPrs761573352
ebirs761573352
HLIrs761573352
Exacrs761573352
Varsomers761573352
Maprs761573352
PheGenIrs761573352
hapmaprs761573352
1000 genomesrs761573352
hgdprs761573352
ensemblrs761573352
gopubmedrs761573352
geneviewrs761573352
scholarrs761573352
googlers761573352
pharmgkbrs761573352
gwascentralrs761573352
openSNPrs761573352
23andMers761573352
23andMe allrs761573352
SNP Nexus

SNPshotrs761573352
SNPdbers761573352
MSV3drs761573352
GWAS Ctlgrs761573352
Max Magnitude0
ClinVar
Risk rs761573352(A;A)
Alt rs761573352(A;A)
Reference rs761573352(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACSF3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89167678G>A
CLNSRC
CLNACC RCV000185756.1,