rs876660073

Orientation

minus

Stabilized

minus

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

Make rs876660073(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

65076639

Gene

MAX

is a	snp
is	mentioned by
dbSNP	rs876660073
dbSNP (classic)	rs876660073
ClinGen	rs876660073
ebi	rs876660073
HLI	rs876660073
Exac	rs876660073
Gnomad	rs876660073
Varsome	rs876660073
LitVar	rs876660073
Map	rs876660073
PheGenI	rs876660073
Biobank	rs876660073
1000 genomes	rs876660073
hgdp	rs876660073
ensembl	rs876660073
geneview	rs876660073
scholar	rs876660073
google	rs876660073
pharmgkb	rs876660073
gwascentral	rs876660073
openSNP	rs876660073
23andMe	rs876660073
SNPshot	rs876660073
SNPdbe	rs876660073
MSV3d	rs876660073
GWAS Ctlg	rs876660073

Max Magnitude

6.2

ClinVar
Risk	rs876660073(A;A)
Alt	rs876660073(A;A)
Reference	Rs876660073(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MAX
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000014.8:g.65543357G>T
CLNSRC
CLNACC	RCV000218866.1,