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rs757789935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757789935(A;G)
Make rs757789935(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position115768306
GeneCASQ2
is asnp
is mentioned by
dbSNPrs757789935
dbSNP (classic)rs757789935
ClinGenrs757789935
ebirs757789935
HLIrs757789935
Exacrs757789935
Gnomadrs757789935
Varsomers757789935
LitVarrs757789935
Maprs757789935
PheGenIrs757789935
Biobankrs757789935
1000 genomesrs757789935
hgdprs757789935
ensemblrs757789935
geneviewrs757789935
scholarrs757789935
googlers757789935
pharmgkbrs757789935
gwascentralrs757789935
openSNPrs757789935
23andMers757789935
23andMe allrs757789935
SNPshotrs757789935
SNPdbers757789935
MSV3drs757789935
GWAS Ctlgrs757789935
Max Magnitude0
ClinVar
Risk rs757789935(G;G)
Alt rs757789935(G;G)
Reference Rs757789935(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CASQ2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.116310927A>G
CLNSRC
CLNACC RCV000489910.1,