rs267608049

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(TC;AG)	6	Lynch syndrome, pathogenic mutation
(TC;TC)	0	common in clinvar

Make rs267608049(AG;AG)

Make rs267608049(AG;TC)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799597

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608049
dbSNP (classic)	rs267608049
ClinGen	rs267608049
ebi	rs267608049
HLI	rs267608049
Exac	rs267608049
Gnomad	rs267608049
Varsome	rs267608049
LitVar	rs267608049
Map	rs267608049
PheGenI	rs267608049
Biobank	rs267608049
1000 genomes	rs267608049
hgdp	rs267608049
ensembl	rs267608049
geneview	rs267608049
scholar	rs267608049
google	rs267608049
pharmgkb	rs267608049
gwascentral	rs267608049
openSNP	rs267608049
23andMe	rs267608049
SNPshot	rs267608049
SNPdbe	rs267608049
MSV3d	rs267608049
GWAS Ctlg	rs267608049

Max Magnitude

6

ClinVar
Risk	rs267608049(AG;AG)
Alt	rs267608049(AG;AG)
Reference	Rs267608049(TC;TC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026736_48026737delTCinsAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074669.2,