rs869025185

Orientation

minus

Stabilized

minus

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

Make rs869025185(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

64805731

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs869025185
dbSNP (classic)	rs869025185
ClinGen	rs869025185
ebi	rs869025185
HLI	rs869025185
Exac	rs869025185
Gnomad	rs869025185
Varsome	rs869025185
LitVar	rs869025185
Map	rs869025185
PheGenI	rs869025185
Biobank	rs869025185
1000 genomes	rs869025185
hgdp	rs869025185
ensembl	rs869025185
geneview	rs869025185
scholar	rs869025185
google	rs869025185
pharmgkb	rs869025185
gwascentral	rs869025185
openSNP	rs869025185
23andMe	rs869025185
SNPshot	rs869025185
SNPdbe	rs869025185
MSV3d	rs869025185
GWAS Ctlg	rs869025185

Max Magnitude

5.8

ClinVar
Risk	rs869025185(-;-)
Alt	rs869025185(-;-)
Reference	Rs869025185(GAG;GAG)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64573203_64573205delCTC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018165.3, RCV000255250.1, RCV000491660.1,