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rs727504157

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504157(G;T)
Make rs727504157(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position73653844
GeneSLC17A5
is asnp
is mentioned by
dbSNPrs727504157
ebirs727504157
HLIrs727504157
Exacrs727504157
Varsomers727504157
Maprs727504157
PheGenIrs727504157
hapmaprs727504157
1000 genomesrs727504157
hgdprs727504157
ensemblrs727504157
gopubmedrs727504157
geneviewrs727504157
scholarrs727504157
googlers727504157
pharmgkbrs727504157
gwascentralrs727504157
openSNPrs727504157
23andMers727504157
23andMe allrs727504157
SNP Nexus

SNPshotrs727504157
SNPdbers727504157
MSV3drs727504157
GWAS Ctlgrs727504157
Max Magnitude0
ClinVar
Risk rs727504157(T;T)
Alt rs727504157(T;T)
Reference rs727504157(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC17A5
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.74363567C>A
CLNSRC
CLNACC RCV000153957.3,