rs1057517764

Orientation

plus

Stabilized

plus

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

Make rs1057517764(-;T)

Make rs1057517764(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47805634

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1057517764
dbSNP (classic)	rs1057517764
ClinGen	rs1057517764
ebi	rs1057517764
HLI	rs1057517764
Exac	rs1057517764
Gnomad	rs1057517764
Varsome	rs1057517764
LitVar	rs1057517764
Map	rs1057517764
PheGenI	rs1057517764
Biobank	rs1057517764
1000 genomes	rs1057517764
hgdp	rs1057517764
ensembl	rs1057517764
geneview	rs1057517764
scholar	rs1057517764
google	rs1057517764
pharmgkb	rs1057517764
gwascentral	rs1057517764
openSNP	rs1057517764
23andMe	rs1057517764
SNPshot	rs1057517764
SNPdbe	rs1057517764
MSV3d	rs1057517764
GWAS Ctlg	rs1057517764

Max Magnitude

0

ClinVar
Risk	rs1057517764(T;T)
Alt	rs1057517764(T;T)
Reference	Rs1057517764(-;-)
Significance	Pathogenic
Disease	not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48032773dupT
CLNSRC
CLNACC	RCV000413655.1, RCV000460316.1, RCV000490868.1,