rs878853824

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Lynch syndrome

Make rs878853824(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47412558

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs878853824
dbSNP (classic)	rs878853824
ClinGen	rs878853824
ebi	rs878853824
HLI	rs878853824
Exac	rs878853824
Gnomad	rs878853824
Varsome	rs878853824
LitVar	rs878853824
Map	rs878853824
PheGenI	rs878853824
Biobank	rs878853824
1000 genomes	rs878853824
hgdp	rs878853824
ensembl	rs878853824
geneview	rs878853824
scholar	rs878853824
google	rs878853824
pharmgkb	rs878853824
gwascentral	rs878853824
openSNP	rs878853824
23andMe	rs878853824
SNPshot	rs878853824
SNPdbe	rs878853824
MSV3d	rs878853824
GWAS Ctlg	rs878853824

Max Magnitude

6

ClinVar
Risk	rs878853824(T;T)
Alt	rs878853824(T;T)
Reference	Rs878853824(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47639697C>T
CLNSRC
CLNACC	RCV000233889.2, RCV000235710.1,