rs63751439

Orientation

plus

Stabilized

plus

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

Make rs63751439(AAGC;AAGC)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017539

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751439
dbSNP (classic)	rs63751439
ClinGen	rs63751439
ebi	rs63751439
HLI	rs63751439
Exac	rs63751439
Gnomad	rs63751439
Varsome	rs63751439
LitVar	rs63751439
Map	rs63751439
PheGenI	rs63751439
Biobank	rs63751439
1000 genomes	rs63751439
hgdp	rs63751439
ensembl	rs63751439
geneview	rs63751439
scholar	rs63751439
google	rs63751439
pharmgkb	rs63751439
gwascentral	rs63751439
openSNP	rs63751439
23andMe	rs63751439
SNPshot	rs63751439
SNPdbe	rs63751439
MSV3d	rs63751439
GWAS Ctlg	rs63751439

Max Magnitude

6

ClinVar
Risk	rs63751439(AAGC;AAGC)
Alt	rs63751439(AAGC;AAGC)
Reference	Rs63751439(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059027_37059030dupAAGC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075879.2,