rs63751431

Orientation

plus

Stabilized

plus

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

Make rs63751431(AATC;AATC)

Reference

GRCh38 38.1/142

Chromosome

3

Position

36996633

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751431
dbSNP (classic)	rs63751431
ClinGen	rs63751431
ebi	rs63751431
HLI	rs63751431
Exac	rs63751431
Gnomad	rs63751431
Varsome	rs63751431
LitVar	rs63751431
Map	rs63751431
PheGenI	rs63751431
Biobank	rs63751431
1000 genomes	rs63751431
hgdp	rs63751431
ensembl	rs63751431
geneview	rs63751431
scholar	rs63751431
google	rs63751431
pharmgkb	rs63751431
gwascentral	rs63751431
openSNP	rs63751431
23andMe	rs63751431
SNPshot	rs63751431
SNPdbe	rs63751431
MSV3d	rs63751431
GWAS Ctlg	rs63751431

Max Magnitude

6

ClinVar
Risk	rs63751431(AATC;AATC)
Alt	rs63751431(AATC;AATC)
Reference	Rs63751431(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038121_37038124dupAATC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075165.2,