rs63751632

Orientation

plus

Stabilized

plus

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

Make rs63751632(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047683

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751632
dbSNP (classic)	rs63751632
ClinGen	rs63751632
ebi	rs63751632
HLI	rs63751632
Exac	rs63751632
Gnomad	rs63751632
Varsome	rs63751632
LitVar	rs63751632
Map	rs63751632
PheGenI	rs63751632
Biobank	rs63751632
1000 genomes	rs63751632
hgdp	rs63751632
ensembl	rs63751632
geneview	rs63751632
scholar	rs63751632
google	rs63751632
pharmgkb	rs63751632
gwascentral	rs63751632
openSNP	rs63751632
23andMe	rs63751632
SNPshot	rs63751632
SNPdbe	rs63751632
MSV3d	rs63751632
GWAS Ctlg	rs63751632

Max Magnitude

6

ClinVar
Risk	rs63751632(A;A)
Alt	rs63751632(A;A)
Reference	Rs63751632(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089174G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075409.2,