rs1057521648

Orientation

minus

Stabilized

minus

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

Make rs1057521648(C;T)

Make rs1057521648(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

127818341

Gene	ENG, LOC102723566

is a	snp
is	mentioned by
dbSNP	rs1057521648
dbSNP (classic)	rs1057521648
ClinGen	rs1057521648
ebi	rs1057521648
HLI	rs1057521648
Exac	rs1057521648
Gnomad	rs1057521648
Varsome	rs1057521648
LitVar	rs1057521648
Map	rs1057521648
PheGenI	rs1057521648
Biobank	rs1057521648
1000 genomes	rs1057521648
hgdp	rs1057521648
ensembl	rs1057521648
geneview	rs1057521648
scholar	rs1057521648
google	rs1057521648
pharmgkb	rs1057521648
gwascentral	rs1057521648
openSNP	rs1057521648
23andMe	rs1057521648
SNPshot	rs1057521648
SNPdbe	rs1057521648
MSV3d	rs1057521648
GWAS Ctlg	rs1057521648

Max Magnitude

0

ClinVar
Risk	rs1057521648(T;T)
Alt	rs1057521648(T;T)
Reference	Rs1057521648(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ENG LOC102723566
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130580620G>A
CLNSRC
CLNACC	RCV000421678.1,