Have questions? Visit https://www.reddit.com/r/SNPedia

rs727504156

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504156(-;-)
Make rs727504156(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position73638492
GeneSLC17A5
is asnp
is mentioned by
dbSNPrs727504156
ebirs727504156
HLIrs727504156
Exacrs727504156
Varsomers727504156
Maprs727504156
PheGenIrs727504156
hapmaprs727504156
1000 genomesrs727504156
hgdprs727504156
ensemblrs727504156
gopubmedrs727504156
geneviewrs727504156
scholarrs727504156
googlers727504156
pharmgkbrs727504156
gwascentralrs727504156
openSNPrs727504156
23andMers727504156
23andMe allrs727504156
SNP Nexus

SNPshotrs727504156
SNPdbers727504156
MSV3drs727504156
GWAS Ctlgrs727504156
Max Magnitude0
ClinVar
Risk rs727504156(;)
Alt rs727504156(;)
Reference rs727504156(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC17A5
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.74348215delG
CLNSRC HGMD
CLNACC RCV000153956.3,