rs757275923

Orientation

plus

Stabilized

plus

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

Make rs757275923(A;A)

Make rs757275923(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

107919017

Gene

DLD

is a	snp
is	mentioned by
dbSNP	rs757275923
dbSNP (classic)	rs757275923
ClinGen	rs757275923
ebi	rs757275923
HLI	rs757275923
Exac	rs757275923
Gnomad	rs757275923
Varsome	rs757275923
LitVar	rs757275923
Map	rs757275923
PheGenI	rs757275923
Biobank	rs757275923
1000 genomes	rs757275923
hgdp	rs757275923
ensembl	rs757275923
geneview	rs757275923
scholar	rs757275923
google	rs757275923
pharmgkb	rs757275923
gwascentral	rs757275923
openSNP	rs757275923
23andMe	rs757275923
SNPshot	rs757275923
SNPdbe	rs757275923
MSV3d	rs757275923
GWAS Ctlg	rs757275923

Max Magnitude

0

ClinVar
Risk	rs757275923(A;A)
Alt	rs757275923(A;A)
Reference	Rs757275923(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DLD
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.107559462G>A
CLNSRC
CLNACC	RCV000185861.1,