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rs750937323

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs750937323(A;G)
Make rs750937323(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position68208178
GeneCLN6
is asnp
is mentioned by
dbSNPrs750937323
dbSNP (old)rs750937323
ClinGenrs750937323
ebirs750937323
HLIrs750937323
Exacrs750937323
Gnomadrs750937323
Varsomers750937323
Maprs750937323
PheGenIrs750937323
Biobankrs750937323
1000 genomesrs750937323
hgdprs750937323
ensemblrs750937323
gopubmedrs750937323
geneviewrs750937323
scholarrs750937323
googlers750937323
pharmgkbrs750937323
gwascentralrs750937323
openSNPrs750937323
23andMers750937323
23andMe allrs750937323
SNP Nexus

SNPshotrs750937323
SNPdbers750937323
MSV3drs750937323
GWAS Ctlgrs750937323
Max Magnitude0
ClinVar
Risk rs750937323(G;G)
Alt rs750937323(G;G)
Reference Rs750937323(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLN6
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.68500516A>G
CLNSRC
CLNACC RCV000416280.1,