rs147810437

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs147810437(C;T)

Make rs147810437(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

179823906

Gene

SQSTM1

is a	snp
is	mentioned by
dbSNP	rs147810437
dbSNP (classic)	rs147810437
ClinGen	rs147810437
ebi	rs147810437
HLI	rs147810437
Exac	rs147810437
Gnomad	rs147810437
Varsome	rs147810437
LitVar	rs147810437
Map	rs147810437
PheGenI	rs147810437
Biobank	rs147810437
1000 genomes	rs147810437
hgdp	rs147810437
ensembl	rs147810437
geneview	rs147810437
scholar	rs147810437
google	rs147810437
pharmgkb	rs147810437
gwascentral	rs147810437
openSNP	rs147810437
23andMe	rs147810437
SNPshot	rs147810437
SNPdbe	rs147810437
MSV3d	rs147810437
GWAS Ctlg	rs147810437

Max Magnitude

0

ClinVar
Risk	rs147810437(T;T)
Alt	rs147810437(T;T)
Reference	Rs147810437(C;C)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	SQSTM1
CLNDBN	not specified
Reversed	0
HGVS	NC_000005.9:g.179250906C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000254519.1,