rs587781773

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;T)	6.2	Hereditary PGL/PCC Syndrome
(T;T)	0	common in clinvar

Make rs587781773(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

96254994

Gene

TMEM127

is a	snp
is	mentioned by
dbSNP	rs587781773
dbSNP (classic)	rs587781773
ClinGen	rs587781773
ebi	rs587781773
HLI	rs587781773
Exac	rs587781773
Gnomad	rs587781773
Varsome	rs587781773
LitVar	rs587781773
Map	rs587781773
PheGenI	rs587781773
Biobank	rs587781773
1000 genomes	rs587781773
hgdp	rs587781773
ensembl	rs587781773
geneview	rs587781773
scholar	rs587781773
google	rs587781773
pharmgkb	rs587781773
gwascentral	rs587781773
openSNP	rs587781773
23andMe	rs587781773
SNPshot	rs587781773
SNPdbe	rs587781773
MSV3d	rs587781773
GWAS Ctlg	rs587781773

Max Magnitude

6.2

ClinVar
Risk	rs587781773(-;-)
Alt	rs587781773(-;-)
Reference	Rs587781773(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TMEM127
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000002.11:g.96920732delA
CLNSRC
CLNACC	RCV000130014.3,