rs1057520733

Orientation

minus

Stabilized

minus

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

Make rs1057520733(C;T)

Make rs1057520733(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64807554

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1057520733
dbSNP (classic)	rs1057520733
ClinGen	rs1057520733
ebi	rs1057520733
HLI	rs1057520733
Exac	rs1057520733
Gnomad	rs1057520733
Varsome	rs1057520733
LitVar	rs1057520733
Map	rs1057520733
PheGenI	rs1057520733
Biobank	rs1057520733
1000 genomes	rs1057520733
hgdp	rs1057520733
ensembl	rs1057520733
geneview	rs1057520733
scholar	rs1057520733
google	rs1057520733
pharmgkb	rs1057520733
gwascentral	rs1057520733
openSNP	rs1057520733
23andMe	rs1057520733
SNPshot	rs1057520733
SNPdbe	rs1057520733
MSV3d	rs1057520733
GWAS Ctlg	rs1057520733

Max Magnitude

0

ClinVar
Risk	rs1057520733(T;T)
Alt	rs1057520733(T;T)
Reference	Rs1057520733(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64575026G>A
CLNSRC
CLNACC	RCV000419478.1,