rs794728618

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;T)	5.8	Multiple Endocrine Neoplasia Type 1

Make rs794728618(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64808030

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs794728618
dbSNP (classic)	rs794728618
ClinGen	rs794728618
ebi	rs794728618
HLI	rs794728618
Exac	rs794728618
Gnomad	rs794728618
Varsome	rs794728618
LitVar	rs794728618
Map	rs794728618
PheGenI	rs794728618
Biobank	rs794728618
1000 genomes	rs794728618
hgdp	rs794728618
ensembl	rs794728618
geneview	rs794728618
scholar	rs794728618
google	rs794728618
pharmgkb	rs794728618
gwascentral	rs794728618
openSNP	rs794728618
23andMe	rs794728618
SNPshot	rs794728618
SNPdbe	rs794728618
MSV3d	rs794728618
GWAS Ctlg	rs794728618

Max Magnitude

5.8

ClinVar
Risk	rs794728618(T;T)
Alt	rs794728618(T;T)
Reference	Rs794728618(A;A)
Significance	Probable-Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64575502T>A
CLNSRC
CLNACC	RCV000182406.2, RCV000492009.1,