rs1057524910

Orientation

plus

Stabilized

plus

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

Make rs1057524910(-;-)

Make rs1057524910(-;GAAA)

Make rs1057524910(GAAA;GAAA)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47471041

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1057524910
dbSNP (classic)	rs1057524910
ClinGen	rs1057524910
ebi	rs1057524910
HLI	rs1057524910
Exac	rs1057524910
Gnomad	rs1057524910
Varsome	rs1057524910
LitVar	rs1057524910
Map	rs1057524910
PheGenI	rs1057524910
Biobank	rs1057524910
1000 genomes	rs1057524910
hgdp	rs1057524910
ensembl	rs1057524910
geneview	rs1057524910
scholar	rs1057524910
google	rs1057524910
pharmgkb	rs1057524910
gwascentral	rs1057524910
openSNP	rs1057524910
23andMe	rs1057524910
SNPshot	rs1057524910
SNPdbe	rs1057524910
MSV3d	rs1057524910
GWAS Ctlg	rs1057524910

Max Magnitude

0

ClinVar
Risk	rs1057524910(-;-)
Alt	rs1057524910(-;-)
Reference	Rs1057524910(AAAG;AAAG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47698180_47698183delGAAA
CLNSRC
CLNACC	RCV000445447.1,