rs104894256

Orientation

minus

Stabilized

minus

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

Make rs104894256(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64810045

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs104894256
dbSNP (classic)	rs104894256
ClinGen	rs104894256
ebi	rs104894256
HLI	rs104894256
Exac	rs104894256
Gnomad	rs104894256
Varsome	rs104894256
LitVar	rs104894256
Map	rs104894256
PheGenI	rs104894256
Biobank	rs104894256
1000 genomes	rs104894256
hgdp	rs104894256
ensembl	rs104894256
geneview	rs104894256
scholar	rs104894256
google	rs104894256
pharmgkb	rs104894256
gwascentral	rs104894256
openSNP	rs104894256
23andMe	rs104894256
SNPshot	rs104894256
SNPdbe	rs104894256
MSV3d	rs104894256
GWAS Ctlg	rs104894256

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894256(G;G)
Alt	rs104894256(G;G)
Reference	Rs104894256(T;T)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia not provided
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 not provided
Reversed	1
HGVS	NC_000011.9:g.64577517A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018157.2, RCV000182402.2,