rs63751301

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GGGA)	6	Lynch syndrome, pathogenic mutation
(GGAG;GGAG)	0	common in clinvar
(GGGA;GGGA)	0	common in clinvar
(I;I)	0

Make rs63751301(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048573

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751301
dbSNP (classic)	rs63751301
ClinGen	rs63751301
ebi	rs63751301
HLI	rs63751301
Exac	rs63751301
Gnomad	rs63751301
Varsome	rs63751301
LitVar	rs63751301
Map	rs63751301
PheGenI	rs63751301
Biobank	rs63751301
1000 genomes	rs63751301
hgdp	rs63751301
ensembl	rs63751301
geneview	rs63751301
scholar	rs63751301
google	rs63751301
pharmgkb	rs63751301
gwascentral	rs63751301
openSNP	rs63751301
23andMe	rs63751301
SNPshot	rs63751301
SNPdbe	rs63751301
MSV3d	rs63751301
GWAS Ctlg	rs63751301

Max Magnitude

6

ClinVar
Risk	rs63751301(-;-)
Alt	rs63751301(-;-)
Reference	Rs63751301(GGAG;GGAG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090064_37090067delGGGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075436.2,