rs794728649

Orientation

minus

Stabilized

minus

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

Make rs794728649(C;C)

Make rs794728649(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64807998

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs794728649
dbSNP (classic)	rs794728649
ClinGen	rs794728649
ebi	rs794728649
HLI	rs794728649
Exac	rs794728649
Gnomad	rs794728649
Varsome	rs794728649
LitVar	rs794728649
Map	rs794728649
PheGenI	rs794728649
Biobank	rs794728649
1000 genomes	rs794728649
hgdp	rs794728649
ensembl	rs794728649
geneview	rs794728649
scholar	rs794728649
google	rs794728649
pharmgkb	rs794728649
gwascentral	rs794728649
openSNP	rs794728649
23andMe	rs794728649
SNPshot	rs794728649
SNPdbe	rs794728649
MSV3d	rs794728649
GWAS Ctlg	rs794728649

Max Magnitude

0

ClinVar
Risk	rs794728649(C;C)
Alt	rs794728649(C;C)
Reference	Rs794728649(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64575470A>G
CLNSRC
CLNACC	RCV000182448.1,