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

rs796052040

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052040(-;-)
Make rs796052040(-;ACAGAAAAAC)
Make rs796052040(ACAGAAAAAC;ACAGAAAAAC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132394202
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs796052040
ebirs796052040
HLIrs796052040
Exacrs796052040
Varsomers796052040
Maprs796052040
PheGenIrs796052040
hapmaprs796052040
1000 genomesrs796052040
hgdprs796052040
ensemblrs796052040
gopubmedrs796052040
geneviewrs796052040
scholarrs796052040
googlers796052040
pharmgkbrs796052040
gwascentralrs796052040
openSNPrs796052040
23andMers796052040
23andMe allrs796052040
SNP Nexus

SNPshotrs796052040
SNPdbers796052040
MSV3drs796052040
GWAS Ctlgrs796052040
Max Magnitude0
ClinVar
Risk rs796052040(AAACACAGAA;AAACACAGAA)
Alt rs796052040(AAACACAGAA;AAACACAGAA)
Reference rs796052040(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131729885_131729894dupACAGAAAAAC
CLNSRC
CLNACC RCV000186158.1,