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rs756260416

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756260416(A;A)
Make rs756260416(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132387066
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs756260416
ebirs756260416
HLIrs756260416
Exacrs756260416
Varsomers756260416
Maprs756260416
PheGenIrs756260416
hapmaprs756260416
1000 genomesrs756260416
hgdprs756260416
ensemblrs756260416
gopubmedrs756260416
geneviewrs756260416
scholarrs756260416
googlers756260416
pharmgkbrs756260416
gwascentralrs756260416
openSNPrs756260416
23andMers756260416
23andMe allrs756260416
SNP Nexus

SNPshotrs756260416
SNPdbers756260416
MSV3drs756260416
GWAS Ctlgrs756260416
Max Magnitude0
ClinVar
Risk rs756260416(A;A)
Alt rs756260416(A;A)
Reference rs756260416(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131722758G>A
CLNSRC
CLNACC RCV000186142.1,