rs786203009

Orientation

minus

Stabilized

minus

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

Make rs786203009(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

65093706

Gene	LOC100506321, MAX

is a	snp
is	mentioned by
dbSNP	rs786203009
dbSNP (classic)	rs786203009
ClinGen	rs786203009
ebi	rs786203009
HLI	rs786203009
Exac	rs786203009
Gnomad	rs786203009
Varsome	rs786203009
LitVar	rs786203009
Map	rs786203009
PheGenI	rs786203009
Biobank	rs786203009
1000 genomes	rs786203009
hgdp	rs786203009
ensembl	rs786203009
geneview	rs786203009
scholar	rs786203009
google	rs786203009
pharmgkb	rs786203009
gwascentral	rs786203009
openSNP	rs786203009
23andMe	rs786203009
SNPshot	rs786203009
SNPdbe	rs786203009
MSV3d	rs786203009
GWAS Ctlg	rs786203009

Max Magnitude

6.2

ClinVar
Risk	rs786203009(A;A)
Alt	rs786203009(A;A)
Reference	Rs786203009(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	LOC100506321 MAX
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000014.8:g.65560424A>T
CLNSRC
CLNACC	RCV000166125.1,