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rs780058786

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs780058786(A;A)
Make rs780058786(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725895
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs780058786
ebirs780058786
HLIrs780058786
Exacrs780058786
Varsomers780058786
Maprs780058786
PheGenIrs780058786
hapmaprs780058786
1000 genomesrs780058786
hgdprs780058786
ensemblrs780058786
gopubmedrs780058786
geneviewrs780058786
scholarrs780058786
googlers780058786
pharmgkbrs780058786
gwascentralrs780058786
openSNPrs780058786
23andMers780058786
23andMe allrs780058786
SNP Nexus

SNPshotrs780058786
SNPdbers780058786
MSV3drs780058786
GWAS Ctlgrs780058786
Max Magnitude0
ClinVar
Risk rs780058786(A;A)
Alt rs780058786(A;A)
Reference rs780058786(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A10
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.45354534G>A
CLNSRC
CLNACC RCV000196028.1,