rs750565190

Orientation

plus

Stabilized

plus

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

Make rs750565190(C;C)

Make rs750565190(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

5741783

Gene

EVC

is a	snp
is	mentioned by
dbSNP	rs750565190
dbSNP (classic)	rs750565190
ClinGen	rs750565190
ebi	rs750565190
HLI	rs750565190
Exac	rs750565190
Gnomad	rs750565190
Varsome	rs750565190
LitVar	rs750565190
Map	rs750565190
PheGenI	rs750565190
Biobank	rs750565190
1000 genomes	rs750565190
hgdp	rs750565190
ensembl	rs750565190
geneview	rs750565190
scholar	rs750565190
google	rs750565190
pharmgkb	rs750565190
gwascentral	rs750565190
openSNP	rs750565190
23andMe	rs750565190
SNPshot	rs750565190
SNPdbe	rs750565190
MSV3d	rs750565190
GWAS Ctlg	rs750565190

Max Magnitude

0

ClinVar
Risk	rs750565190(A;A) rs750565190(C;C)
Alt	rs750565190(A;A) rs750565190(C;C)
Reference	Rs750565190(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	EVC
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.5743510T>A
CLNSRC
CLNACC	RCV000171373.1,