rs1060499984

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1060499984(C;G)

Make rs1060499984(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64805643

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499984
dbSNP (classic)	rs1060499984
ClinGen	rs1060499984
ebi	rs1060499984
HLI	rs1060499984
Exac	rs1060499984
Gnomad	rs1060499984
Varsome	rs1060499984
LitVar	rs1060499984
Map	rs1060499984
PheGenI	rs1060499984
Biobank	rs1060499984
1000 genomes	rs1060499984
hgdp	rs1060499984
ensembl	rs1060499984
geneview	rs1060499984
scholar	rs1060499984
google	rs1060499984
pharmgkb	rs1060499984
gwascentral	rs1060499984
openSNP	rs1060499984
23andMe	rs1060499984
SNPshot	rs1060499984
SNPdbe	rs1060499984
MSV3d	rs1060499984
GWAS Ctlg	rs1060499984

Max Magnitude

0

ClinVar
Risk	rs1060499984(G;G) rs1060499984(T;T)
Alt	rs1060499984(G;G) rs1060499984(T;T)
Reference	Rs1060499984(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64573115G>A; NC_000011.9:g.64573115G>C
CLNSRC
CLNACC	RCV000491380.1, RCV000472220.1,