rs587781931

Orientation

minus

Stabilized

minus

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

Make rs587781931(-;A)

Make rs587781931(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

65077974

Gene

MAX

is a	snp
is	mentioned by
dbSNP	rs587781931
dbSNP (classic)	rs587781931
ClinGen	rs587781931
ebi	rs587781931
HLI	rs587781931
Exac	rs587781931
Gnomad	rs587781931
Varsome	rs587781931
LitVar	rs587781931
Map	rs587781931
PheGenI	rs587781931
Biobank	rs587781931
1000 genomes	rs587781931
hgdp	rs587781931
ensembl	rs587781931
geneview	rs587781931
scholar	rs587781931
google	rs587781931
pharmgkb	rs587781931
gwascentral	rs587781931
openSNP	rs587781931
23andMe	rs587781931
SNPshot	rs587781931
SNPdbe	rs587781931
MSV3d	rs587781931
GWAS Ctlg	rs587781931

Max Magnitude

0

ClinVar
Risk	rs587781931(A;A)
Alt	rs587781931(A;A)
Reference	Rs587781931(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MAX
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000014.8:g.65544693dupT
CLNSRC
CLNACC	RCV000130290.2,