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

rs771156053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs771156053(-;-)
Make rs771156053(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position73621877
GeneSLC17A5
is asnp
is mentioned by
dbSNPrs771156053
dbSNP (classic)rs771156053
ClinGenrs771156053
ebirs771156053
HLIrs771156053
Exacrs771156053
Gnomadrs771156053
Varsomers771156053
LitVarrs771156053
Maprs771156053
PheGenIrs771156053
Biobankrs771156053
1000 genomesrs771156053
hgdprs771156053
ensemblrs771156053
geneviewrs771156053
scholarrs771156053
googlers771156053
pharmgkbrs771156053
gwascentralrs771156053
openSNPrs771156053
23andMers771156053
23andMe allrs771156053
SNPshotrs771156053
SNPdbers771156053
MSV3drs771156053
GWAS Ctlgrs771156053
Max Magnitude0
ClinVar
Risk rs771156053(-;-)
Alt rs771156053(-;-)
Reference Rs771156053(T;T)
Significance Probable-Pathogenic
Disease Salla disease
Variation info
Gene SLC17A5
CLNDBN Salla disease
Reversed 0
HGVS NC_000006.11:g.74331600delT
CLNSRC
CLNACC RCV000409422.1,