rs869312167

Orientation

minus

Stabilized

minus

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

Make rs869312167(-;-)

Make rs869312167(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

64809958

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs869312167
dbSNP (classic)	rs869312167
ClinGen	rs869312167
ebi	rs869312167
HLI	rs869312167
Exac	rs869312167
Gnomad	rs869312167
Varsome	rs869312167
LitVar	rs869312167
Map	rs869312167
PheGenI	rs869312167
Biobank	rs869312167
1000 genomes	rs869312167
hgdp	rs869312167
ensembl	rs869312167
geneview	rs869312167
scholar	rs869312167
google	rs869312167
pharmgkb	rs869312167
gwascentral	rs869312167
openSNP	rs869312167
23andMe	rs869312167
SNPshot	rs869312167
SNPdbe	rs869312167
MSV3d	rs869312167
GWAS Ctlg	rs869312167

Max Magnitude

0

ClinVar
Risk	rs869312167(-;-)
Alt	rs869312167(-;-)
Reference	Rs869312167(A;A)
Significance	Pathogenic
Disease	Primary hyperparathyroidism
Variation	info
Gene	MEN1
CLNDBN	Primary hyperparathyroidism
Reversed	1
HGVS	NC_000011.9:g.64577430delT
CLNSRC
CLNACC	RCV000210355.1,