rs1057520605

Orientation

plus

Stabilized

plus

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

Make rs1057520605(G;T)

Make rs1057520605(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47798839

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1057520605
dbSNP (classic)	rs1057520605
ClinGen	rs1057520605
ebi	rs1057520605
HLI	rs1057520605
Exac	rs1057520605
Gnomad	rs1057520605
Varsome	rs1057520605
LitVar	rs1057520605
Map	rs1057520605
PheGenI	rs1057520605
Biobank	rs1057520605
1000 genomes	rs1057520605
hgdp	rs1057520605
ensembl	rs1057520605
geneview	rs1057520605
scholar	rs1057520605
google	rs1057520605
pharmgkb	rs1057520605
gwascentral	rs1057520605
openSNP	rs1057520605
23andMe	rs1057520605
SNPshot	rs1057520605
SNPdbe	rs1057520605
MSV3d	rs1057520605
GWAS Ctlg	rs1057520605

Max Magnitude

0

ClinVar
Risk	rs1057520605(T;T)
Alt	rs1057520605(T;T)
Reference	Rs1057520605(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH6
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.48025978G>T
CLNSRC
CLNACC	RCV000441289.1,