rs104894265

Orientation

minus

Stabilized

minus

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

Make rs104894265(A;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64805758

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs104894265
dbSNP (classic)	rs104894265
ClinGen	rs104894265
ebi	rs104894265
HLI	rs104894265
Exac	rs104894265
Gnomad	rs104894265
Varsome	rs104894265
LitVar	rs104894265
Map	rs104894265
PheGenI	rs104894265
Biobank	rs104894265
1000 genomes	rs104894265
hgdp	rs104894265
ensembl	rs104894265
geneview	rs104894265
scholar	rs104894265
google	rs104894265
pharmgkb	rs104894265
gwascentral	rs104894265
openSNP	rs104894265
23andMe	rs104894265
SNPshot	rs104894265
SNPdbe	rs104894265
MSV3d	rs104894265
GWAS Ctlg	rs104894265

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0029
Related	also

ClinVar
Risk	rs104894265(A;A)
Alt	rs104894265(A;A)
Reference	Rs104894265(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64573230G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018185.3,