rs63751167

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;GTGA)	6	Lynch syndrome, pathogenic mutation
(D;D)	0

Make rs63751167(GTGA;GTGA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799943

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63751167
dbSNP (classic)	rs63751167
ClinGen	rs63751167
ebi	rs63751167
HLI	rs63751167
Exac	rs63751167
Gnomad	rs63751167
Varsome	rs63751167
LitVar	rs63751167
Map	rs63751167
PheGenI	rs63751167
Biobank	rs63751167
1000 genomes	rs63751167
hgdp	rs63751167
ensembl	rs63751167
geneview	rs63751167
scholar	rs63751167
google	rs63751167
pharmgkb	rs63751167
gwascentral	rs63751167
openSNP	rs63751167
23andMe	rs63751167
SNPshot	rs63751167
SNPdbe	rs63751167
MSV3d	rs63751167
GWAS Ctlg	rs63751167

Max Magnitude

6

ClinVar
Risk	rs63751167(GTGA;GTGA)
Alt	rs63751167(GTGA;GTGA)
Reference	Rs63751167(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027079_48027082dupGTGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074699.2,