rs876659610

Orientation

minus

Stabilized

minus

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

Make rs876659610(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

65077996

Gene

MAX

is a	snp
is	mentioned by
dbSNP	rs876659610
dbSNP (classic)	rs876659610
ClinGen	rs876659610
ebi	rs876659610
HLI	rs876659610
Exac	rs876659610
Gnomad	rs876659610
Varsome	rs876659610
LitVar	rs876659610
Map	rs876659610
PheGenI	rs876659610
Biobank	rs876659610
1000 genomes	rs876659610
hgdp	rs876659610
ensembl	rs876659610
geneview	rs876659610
scholar	rs876659610
google	rs876659610
pharmgkb	rs876659610
gwascentral	rs876659610
openSNP	rs876659610
23andMe	rs876659610
SNPshot	rs876659610
SNPdbe	rs876659610
MSV3d	rs876659610
GWAS Ctlg	rs876659610

Max Magnitude

6.2

ClinVar
Risk	rs876659610(A;A)
Alt	rs876659610(A;A)
Reference	Rs876659610(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MAX
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000014.8:g.65544714A>T
CLNSRC
CLNACC	RCV000222188.1,