rs748026507

Orientation

plus

Stabilized

plus

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

Make rs748026507(C;C)

Make rs748026507(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

40407992

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs748026507
dbSNP (classic)	rs748026507
ClinGen	rs748026507
ebi	rs748026507
HLI	rs748026507
Exac	rs748026507
Gnomad	rs748026507
Varsome	rs748026507
LitVar	rs748026507
Map	rs748026507
PheGenI	rs748026507
Biobank	rs748026507
1000 genomes	rs748026507
hgdp	rs748026507
ensembl	rs748026507
geneview	rs748026507
scholar	rs748026507
google	rs748026507
pharmgkb	rs748026507
gwascentral	rs748026507
openSNP	rs748026507
23andMe	rs748026507
SNPshot	rs748026507
SNPdbe	rs748026507
MSV3d	rs748026507
GWAS Ctlg	rs748026507

Max Magnitude

0

ClinVar
Risk	rs748026507(C;C)
Alt	rs748026507(C;C)
Reference	Rs748026507(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40700191T>C
CLNSRC
CLNACC	RCV000185982.1,