rs104894262

Orientation

minus

Stabilized

minus

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

Make rs104894262(A;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64807994

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs104894262
dbSNP (classic)	rs104894262
ClinGen	rs104894262
ebi	rs104894262
HLI	rs104894262
Exac	rs104894262
Gnomad	rs104894262
Varsome	rs104894262
LitVar	rs104894262
Map	rs104894262
PheGenI	rs104894262
Biobank	rs104894262
1000 genomes	rs104894262
hgdp	rs104894262
ensembl	rs104894262
geneview	rs104894262
scholar	rs104894262
google	rs104894262
pharmgkb	rs104894262
gwascentral	rs104894262
openSNP	rs104894262
23andMe	rs104894262
SNPshot	rs104894262
SNPdbe	rs104894262
MSV3d	rs104894262
GWAS Ctlg	rs104894262

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0021
Related	also

ClinVar
Risk	rs104894262(A;A)
Alt	rs104894262(A;A)
Reference	Rs104894262(T;T)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64575466A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018177.3,