rs1060499992

Orientation

minus

Stabilized

minus

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

Make rs1060499992(G;T)

Make rs1060499992(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64809764

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499992
dbSNP (classic)	rs1060499992
ClinGen	rs1060499992
ebi	rs1060499992
HLI	rs1060499992
Exac	rs1060499992
Gnomad	rs1060499992
Varsome	rs1060499992
LitVar	rs1060499992
Map	rs1060499992
PheGenI	rs1060499992
Biobank	rs1060499992
1000 genomes	rs1060499992
hgdp	rs1060499992
ensembl	rs1060499992
geneview	rs1060499992
scholar	rs1060499992
google	rs1060499992
pharmgkb	rs1060499992
gwascentral	rs1060499992
openSNP	rs1060499992
23andMe	rs1060499992
SNPshot	rs1060499992
SNPdbe	rs1060499992
MSV3d	rs1060499992
GWAS Ctlg	rs1060499992

Max Magnitude

0

ClinVar
Risk	rs1060499992(T;T)
Alt	rs1060499992(T;T)
Reference	Rs1060499992(G;G)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64577236C>A
CLNSRC
CLNACC	RCV000469372.1,