rs864622436

Orientation

plus

Stabilized

plus

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

Make rs864622436(-;-)

Make rs864622436(-;TTCGATTTGCAGCAAATTGACTTCTTTA)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47470953

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs864622436
dbSNP (classic)	rs864622436
ClinGen	rs864622436
ebi	rs864622436
HLI	rs864622436
Exac	rs864622436
Gnomad	rs864622436
Varsome	rs864622436
LitVar	rs864622436
Map	rs864622436
PheGenI	rs864622436
Biobank	rs864622436
1000 genomes	rs864622436
hgdp	rs864622436
ensembl	rs864622436
geneview	rs864622436
scholar	rs864622436
google	rs864622436
pharmgkb	rs864622436
gwascentral	rs864622436
openSNP	rs864622436
23andMe	rs864622436
SNPshot	rs864622436
SNPdbe	rs864622436
MSV3d	rs864622436
GWAS Ctlg	rs864622436

Max Magnitude

0

ClinVar
Risk	rs864622436(-;-)
Alt	rs864622436(-;-)
Reference	Rs864622436(TTCGATTTGCAGCAAATTGACTTCTTTA;TTCGATTTGCAGCAAATTGACTTCTTTA)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47698092_47698119del28
CLNSRC
CLNACC	RCV000204865.2,