rs786205215

Orientation

minus

Stabilized

minus

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

Make rs786205215(C;T)

Make rs786205215(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58363582

Gene

RNF43

is a	snp
is	mentioned by
dbSNP	rs786205215
dbSNP (classic)	rs786205215
ClinGen	rs786205215
ebi	rs786205215
HLI	rs786205215
Exac	rs786205215
Gnomad	rs786205215
Varsome	rs786205215
LitVar	rs786205215
Map	rs786205215
PheGenI	rs786205215
Biobank	rs786205215
1000 genomes	rs786205215
hgdp	rs786205215
ensembl	rs786205215
geneview	rs786205215
scholar	rs786205215
google	rs786205215
pharmgkb	rs786205215
gwascentral	rs786205215
openSNP	rs786205215
23andMe	rs786205215
SNPshot	rs786205215
SNPdbe	rs786205215
MSV3d	rs786205215
GWAS Ctlg	rs786205215

Max Magnitude

0

ClinVar
Risk	rs786205215(T;T)
Alt	rs786205215(T;T)
Reference	Rs786205215(C;C)
Significance	Pathogenic
Disease	Colon Serrated Polyposis Sessile serrated polyposis cancer syndrome
Variation	info
Gene	RNF43
CLNDBN	Colon Serrated Polyposis Sessile serrated polyposis cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.56440943G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170445.1, RCV000240616.1,