rs794728617

Orientation

minus

Stabilized

minus

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

Make rs794728617(A;A)

Make rs794728617(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64808072

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs794728617
dbSNP (classic)	rs794728617
ClinGen	rs794728617
ebi	rs794728617
HLI	rs794728617
Exac	rs794728617
Gnomad	rs794728617
Varsome	rs794728617
LitVar	rs794728617
Map	rs794728617
PheGenI	rs794728617
Biobank	rs794728617
1000 genomes	rs794728617
hgdp	rs794728617
ensembl	rs794728617
geneview	rs794728617
scholar	rs794728617
google	rs794728617
pharmgkb	rs794728617
gwascentral	rs794728617
openSNP	rs794728617
23andMe	rs794728617
SNPshot	rs794728617
SNPdbe	rs794728617
MSV3d	rs794728617
GWAS Ctlg	rs794728617

Max Magnitude

0

ClinVar
Risk	rs794728617(A;A) rs794728617(T;T)
Alt	rs794728617(A;A) rs794728617(T;T)
Reference	Rs794728617(C;C)
Significance	Probable-Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64575544G>T
CLNSRC
CLNACC	RCV000474814.1,