rs200862792

Orientation

plus

Stabilized

plus

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

Make rs200862792(A;A)

Make rs200862792(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74056402

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs200862792
dbSNP (classic)	rs200862792
ClinGen	rs200862792
ebi	rs200862792
HLI	rs200862792
Exac	rs200862792
Gnomad	rs200862792
Varsome	rs200862792
LitVar	rs200862792
Map	rs200862792
PheGenI	rs200862792
Biobank	rs200862792
1000 genomes	rs200862792
hgdp	rs200862792
ensembl	rs200862792
geneview	rs200862792
scholar	rs200862792
google	rs200862792
pharmgkb	rs200862792
gwascentral	rs200862792
openSNP	rs200862792
23andMe	rs200862792
SNPshot	rs200862792
SNPdbe	rs200862792
MSV3d	rs200862792
GWAS Ctlg	rs200862792

Max Magnitude

0

ClinVar
Risk	rs200862792(A;A) rs200862792(T;T)
Alt	rs200862792(A;A) rs200862792(T;T)
Reference	Rs200862792(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73470732G>T
CLNSRC
CLNACC	RCV000196367.1,