rs376872829

Orientation

plus

Stabilized

plus

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

Make rs376872829(A;A)

Make rs376872829(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64808019

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs376872829
dbSNP (classic)	rs376872829
ClinGen	rs376872829
ebi	rs376872829
HLI	rs376872829
Exac	rs376872829
Gnomad	rs376872829
Varsome	rs376872829
LitVar	rs376872829
Map	rs376872829
PheGenI	rs376872829
Biobank	rs376872829
1000 genomes	rs376872829
hgdp	rs376872829
ensembl	rs376872829
geneview	rs376872829
scholar	rs376872829
google	rs376872829
pharmgkb	rs376872829
gwascentral	rs376872829
openSNP	rs376872829
23andMe	rs376872829
SNPshot	rs376872829
SNPdbe	rs376872829
MSV3d	rs376872829
GWAS Ctlg	rs376872829

Max Magnitude

5.8

ClinVar
Risk	rs376872829(A;A) rs376872829(G;G)
Alt	rs376872829(A;A) rs376872829(G;G)
Reference	Rs376872829(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.64575491C>G
CLNSRC
CLNACC	RCV000491572.1,