rs794728648

Orientation

minus

Stabilized

minus

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

Make rs794728648(G;T)

Make rs794728648(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64808078

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs794728648
dbSNP (classic)	rs794728648
ClinGen	rs794728648
ebi	rs794728648
HLI	rs794728648
Exac	rs794728648
Gnomad	rs794728648
Varsome	rs794728648
LitVar	rs794728648
Map	rs794728648
PheGenI	rs794728648
Biobank	rs794728648
1000 genomes	rs794728648
hgdp	rs794728648
ensembl	rs794728648
geneview	rs794728648
scholar	rs794728648
google	rs794728648
pharmgkb	rs794728648
gwascentral	rs794728648
openSNP	rs794728648
23andMe	rs794728648
SNPshot	rs794728648
SNPdbe	rs794728648
MSV3d	rs794728648
GWAS Ctlg	rs794728648

Max Magnitude

0

ClinVar
Risk	rs794728648(A;A) rs794728648(T;T)
Alt	rs794728648(A;A) rs794728648(T;T)
Reference	Rs794728648(G;G)
Significance	Pathogenic
Disease	not provided Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	not provided Multiple endocrine neoplasia, type 1 Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64575550C>T
CLNSRC
CLNACC	RCV000425558.1, RCV000466874.1, RCV000491482.1,