rs587781628

Orientation

minus

Stabilized

minus

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

Make rs587781628(A;G)

Make rs587781628(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

45331558

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs587781628
dbSNP (classic)	rs587781628
ClinGen	rs587781628
ebi	rs587781628
HLI	rs587781628
Exac	rs587781628
Gnomad	rs587781628
Varsome	rs587781628
LitVar	rs587781628
Map	rs587781628
PheGenI	rs587781628
Biobank	rs587781628
1000 genomes	rs587781628
hgdp	rs587781628
ensembl	rs587781628
geneview	rs587781628
scholar	rs587781628
google	rs587781628
pharmgkb	rs587781628
gwascentral	rs587781628
openSNP	rs587781628
23andMe	rs587781628
SNPshot	rs587781628
SNPdbe	rs587781628
MSV3d	rs587781628
GWAS Ctlg	rs587781628

Max Magnitude

0

ClinVar
Risk	rs587781628(G;G)
Alt	rs587781628(G;G)
Reference	Rs587781628(A;A)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Carcinoma of colon MYH-associated polyposis not provided
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome Carcinoma of colon MYH-associated polyposis not provided
Reversed	1
HGVS	NC_000001.10:g.45797230T>C
CLNSRC
CLNACC	RCV000129730.4, RCV000172819.1, RCV000338621.1, RCV000480885.1,