rs104894258

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	5.8	Multiple Endocrine Neoplasia Type 1
(G;G)	0	common in complete genomics

Make rs104894258(A;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64807952

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs104894258
dbSNP (classic)	rs104894258
ClinGen	rs104894258
ebi	rs104894258
HLI	rs104894258
Exac	rs104894258
Gnomad	rs104894258
Varsome	rs104894258
LitVar	rs104894258
Map	rs104894258
PheGenI	rs104894258
Biobank	rs104894258
1000 genomes	rs104894258
hgdp	rs104894258
ensembl	rs104894258
geneview	rs104894258
scholar	rs104894258
google	rs104894258
pharmgkb	rs104894258
gwascentral	rs104894258
openSNP	rs104894258
23andMe	rs104894258
SNPshot	rs104894258
SNPdbe	rs104894258
MSV3d	rs104894258
GWAS Ctlg	rs104894258

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894258(A;A)
Alt	rs104894258(A;A)
Reference	Rs104894258(G;G)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64575424C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018162.2,