rs1057517760

Orientation

minus

Stabilized

minus

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

Make rs1057517760(-;AGC)

Make rs1057517760(AGC;AGC)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64807559

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1057517760
dbSNP (classic)	rs1057517760
ClinGen	rs1057517760
ebi	rs1057517760
HLI	rs1057517760
Exac	rs1057517760
Gnomad	rs1057517760
Varsome	rs1057517760
LitVar	rs1057517760
Map	rs1057517760
PheGenI	rs1057517760
Biobank	rs1057517760
1000 genomes	rs1057517760
hgdp	rs1057517760
ensembl	rs1057517760
geneview	rs1057517760
scholar	rs1057517760
google	rs1057517760
pharmgkb	rs1057517760
gwascentral	rs1057517760
openSNP	rs1057517760
23andMe	rs1057517760
SNPshot	rs1057517760
SNPdbe	rs1057517760
MSV3d	rs1057517760
GWAS Ctlg	rs1057517760

Max Magnitude

0

ClinVar
Risk	rs1057517760(AGC;AGC)
Alt	rs1057517760(AGC;AGC)
Reference	Rs1057517760(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64575032_64575034dupGCT
CLNSRC
CLNACC	RCV000412812.1,