rs1057517899

Orientation

plus

Stabilized

plus

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

Make rs1057517899(C;T)

Make rs1057517899(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

5711552

Gene

EVC

is a	snp
is	mentioned by
dbSNP	rs1057517899
dbSNP (classic)	rs1057517899
ClinGen	rs1057517899
ebi	rs1057517899
HLI	rs1057517899
Exac	rs1057517899
Gnomad	rs1057517899
Varsome	rs1057517899
LitVar	rs1057517899
Map	rs1057517899
PheGenI	rs1057517899
Biobank	rs1057517899
1000 genomes	rs1057517899
hgdp	rs1057517899
ensembl	rs1057517899
geneview	rs1057517899
scholar	rs1057517899
google	rs1057517899
pharmgkb	rs1057517899
gwascentral	rs1057517899
openSNP	rs1057517899
23andMe	rs1057517899
SNPshot	rs1057517899
SNPdbe	rs1057517899
MSV3d	rs1057517899
GWAS Ctlg	rs1057517899

Max Magnitude

0

ClinVar
Risk	rs1057517899(T;T)
Alt	rs1057517899(T;T)
Reference	Rs1057517899(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	EVC
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.5713279C>T
CLNSRC
CLNACC	RCV000413234.1,