rs397515385

Orientation

minus

Stabilized

minus

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

Make rs397515385(-;-)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64809708

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs397515385
dbSNP (classic)	rs397515385
ClinGen	rs397515385
ebi	rs397515385
HLI	rs397515385
Exac	rs397515385
Gnomad	rs397515385
Varsome	rs397515385
LitVar	rs397515385
Map	rs397515385
PheGenI	rs397515385
Biobank	rs397515385
1000 genomes	rs397515385
hgdp	rs397515385
ensembl	rs397515385
geneview	rs397515385
scholar	rs397515385
google	rs397515385
pharmgkb	rs397515385
gwascentral	rs397515385
openSNP	rs397515385
23andMe	rs397515385
SNPshot	rs397515385
SNPdbe	rs397515385
MSV3d	rs397515385
GWAS Ctlg	rs397515385

Max Magnitude

5.8

ClinVar
Risk	rs397515385(-;-)
Alt	rs397515385(-;-)
Reference	Rs397515385(C;C)
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.64577180delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018161.3, RCV000182436.1, RCV000491332.1,