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

rs796051870

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051870(A;A)
Make rs796051870(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position179833783
GeneSQSTM1
is asnp
is mentioned by
dbSNPrs796051870
ebirs796051870
HLIrs796051870
Exacrs796051870
Varsomers796051870
Maprs796051870
PheGenIrs796051870
hapmaprs796051870
1000 genomesrs796051870
hgdprs796051870
ensemblrs796051870
gopubmedrs796051870
geneviewrs796051870
scholarrs796051870
googlers796051870
pharmgkbrs796051870
gwascentralrs796051870
openSNPrs796051870
23andMers796051870
23andMe allrs796051870
SNP Nexus

SNPshotrs796051870
SNPdbers796051870
MSV3drs796051870
GWAS Ctlgrs796051870
Max Magnitude0
ClinVar
Risk rs796051870(A;A)
Alt rs796051870(A;A)
Reference rs796051870(G;G)
Significance Pathogenic
Disease Paget disease of bone
Variation info
Gene SQSTM1
CLNDBN Paget disease of bone, familial
Reversed 0
HGVS NC_000005.9:g.179260783G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008578.3,