rs794728651

Orientation

minus

Stabilized

minus

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

Make rs794728651(A;C)

Make rs794728651(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64807664

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs794728651
dbSNP (classic)	rs794728651
ClinGen	rs794728651
ebi	rs794728651
HLI	rs794728651
Exac	rs794728651
Gnomad	rs794728651
Varsome	rs794728651
LitVar	rs794728651
Map	rs794728651
PheGenI	rs794728651
Biobank	rs794728651
1000 genomes	rs794728651
hgdp	rs794728651
ensembl	rs794728651
geneview	rs794728651
scholar	rs794728651
google	rs794728651
pharmgkb	rs794728651
gwascentral	rs794728651
openSNP	rs794728651
23andMe	rs794728651
SNPshot	rs794728651
SNPdbe	rs794728651
MSV3d	rs794728651
GWAS Ctlg	rs794728651

Max Magnitude

0

ClinVar
Risk	rs794728651(C;C)
Alt	rs794728651(C;C)
Reference	Rs794728651(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64575136T>G
CLNSRC
CLNACC	RCV000182451.1,