rs750115837

Orientation

plus

Stabilized

plus

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

Make rs750115837(A;G)

Make rs750115837(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

127826659

Gene	ENG, LOC105379841

is a	snp
is	mentioned by
dbSNP	rs750115837
dbSNP (classic)	rs750115837
ClinGen	rs750115837
ebi	rs750115837
HLI	rs750115837
Exac	rs750115837
Gnomad	rs750115837
Varsome	rs750115837
LitVar	rs750115837
Map	rs750115837
PheGenI	rs750115837
Biobank	rs750115837
1000 genomes	rs750115837
hgdp	rs750115837
ensembl	rs750115837
geneview	rs750115837
scholar	rs750115837
google	rs750115837
pharmgkb	rs750115837
gwascentral	rs750115837
openSNP	rs750115837
23andMe	rs750115837
SNPshot	rs750115837
SNPdbe	rs750115837
MSV3d	rs750115837
GWAS Ctlg	rs750115837

Max Magnitude

0

ClinVar
Risk	rs750115837(G;G)
Alt	rs750115837(G;G)
Reference	Rs750115837(A;A)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	ENG
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000009.11:g.130588938A>G; NC_000009.11:g.130588938A>T
CLNSRC
CLNACC	RCV000455548.1, RCV000493483.1,