rs398123698

Orientation

minus

Stabilized

minus

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

Make rs398123698(A;A)

Make rs398123698(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

20348252

Gene

UMOD

is a	snp
is	mentioned by
dbSNP	rs398123698
dbSNP (classic)	rs398123698
ClinGen	rs398123698
ebi	rs398123698
HLI	rs398123698
Exac	rs398123698
Gnomad	rs398123698
Varsome	rs398123698
LitVar	rs398123698
Map	rs398123698
PheGenI	rs398123698
Biobank	rs398123698
1000 genomes	rs398123698
hgdp	rs398123698
ensembl	rs398123698
geneview	rs398123698
scholar	rs398123698
google	rs398123698
pharmgkb	rs398123698
gwascentral	rs398123698
openSNP	rs398123698
23andMe	rs398123698
SNPshot	rs398123698
SNPdbe	rs398123698
MSV3d	rs398123698
GWAS Ctlg	rs398123698

Max Magnitude

0

ClinVar
Risk	rs398123698(A;A)
Alt	rs398123698(A;A)
Reference	Rs398123698(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	UMOD
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.20359574C>T
CLNSRC	HGMD
CLNACC	RCV000080096.4,