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rs762610288

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762610288(A;A)
Make rs762610288(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position137236239
GeneSLC34A3
is asnp
is mentioned by
dbSNPrs762610288
dbSNP (classic)rs762610288
ClinGenrs762610288
ebirs762610288
HLIrs762610288
Exacrs762610288
Gnomadrs762610288
Varsomers762610288
LitVarrs762610288
Maprs762610288
PheGenIrs762610288
Biobankrs762610288
1000 genomesrs762610288
hgdprs762610288
ensemblrs762610288
geneviewrs762610288
scholarrs762610288
googlers762610288
pharmgkbrs762610288
gwascentralrs762610288
openSNPrs762610288
23andMers762610288
SNPshotrs762610288
SNPdbers762610288
MSV3drs762610288
GWAS Ctlgrs762610288
Max Magnitude0
ClinVar
Risk rs762610288(A;A)
Alt rs762610288(A;A)
Reference Rs762610288(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC34A3
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140130691G>A
CLNSRC
CLNACC RCV000484421.1,