rs1057517762

Orientation

plus

Stabilized

plus

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

Make rs1057517762(-;-)

Make rs1057517762(-;TCTTAACCGA)

Make rs1057517762(TCTTAACCGA;TCTTAACCGA)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47429823

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1057517762
dbSNP (classic)	rs1057517762
ClinGen	rs1057517762
ebi	rs1057517762
HLI	rs1057517762
Exac	rs1057517762
Gnomad	rs1057517762
Varsome	rs1057517762
LitVar	rs1057517762
Map	rs1057517762
PheGenI	rs1057517762
Biobank	rs1057517762
1000 genomes	rs1057517762
hgdp	rs1057517762
ensembl	rs1057517762
geneview	rs1057517762
scholar	rs1057517762
google	rs1057517762
pharmgkb	rs1057517762
gwascentral	rs1057517762
openSNP	rs1057517762
23andMe	rs1057517762
SNPshot	rs1057517762
SNPdbe	rs1057517762
MSV3d	rs1057517762
GWAS Ctlg	rs1057517762

Max Magnitude

0

ClinVar
Risk	rs1057517762(-;-)
Alt	rs1057517762(-;-)
Reference	Rs1057517762(GATCTTAACC;GATCTTAACC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47656962_47656971delTCTTAACCGA
CLNSRC
CLNACC	RCV000413539.1,