rs747273828

Orientation

plus

Stabilized

plus

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

Make rs747273828(C;C)

Make rs747273828(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

40407696

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs747273828
dbSNP (classic)	rs747273828
ClinGen	rs747273828
ebi	rs747273828
HLI	rs747273828
Exac	rs747273828
Gnomad	rs747273828
Varsome	rs747273828
LitVar	rs747273828
Map	rs747273828
PheGenI	rs747273828
Biobank	rs747273828
1000 genomes	rs747273828
hgdp	rs747273828
ensembl	rs747273828
geneview	rs747273828
scholar	rs747273828
google	rs747273828
pharmgkb	rs747273828
gwascentral	rs747273828
openSNP	rs747273828
23andMe	rs747273828
SNPshot	rs747273828
SNPdbe	rs747273828
MSV3d	rs747273828
GWAS Ctlg	rs747273828

Max Magnitude

0

ClinVar
Risk	rs747273828(A;A) rs747273828(C;C)
Alt	rs747273828(A;A) rs747273828(C;C)
Reference	Rs747273828(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40699897G>A; NC_000015.9:g.40699897G>C
CLNSRC
CLNACC	RCV000185979.1, RCV000185980.1,