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rs777004046

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs777004046(A;C)
Make rs777004046(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position132390688
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs777004046
ebirs777004046
HLIrs777004046
Exacrs777004046
Varsomers777004046
Maprs777004046
PheGenIrs777004046
hapmaprs777004046
1000 genomesrs777004046
hgdprs777004046
ensemblrs777004046
gopubmedrs777004046
geneviewrs777004046
scholarrs777004046
googlers777004046
pharmgkbrs777004046
gwascentralrs777004046
openSNPrs777004046
23andMers777004046
23andMe allrs777004046
SNP Nexus

SNPshotrs777004046
SNPdbers777004046
MSV3drs777004046
GWAS Ctlgrs777004046
Max Magnitude0
ClinVar
Risk rs777004046(C;C)
Alt rs777004046(C;C)
Reference rs777004046(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131726380A>C
CLNSRC
CLNACC RCV000186143.1,