rs63750814

Orientation

plus

Stabilized

plus

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

Make rs63750814(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017575

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750814
dbSNP (classic)	rs63750814
ClinGen	rs63750814
ebi	rs63750814
HLI	rs63750814
Exac	rs63750814
Gnomad	rs63750814
Varsome	rs63750814
LitVar	rs63750814
Map	rs63750814
PheGenI	rs63750814
Biobank	rs63750814
1000 genomes	rs63750814
hgdp	rs63750814
ensembl	rs63750814
geneview	rs63750814
scholar	rs63750814
google	rs63750814
pharmgkb	rs63750814
gwascentral	rs63750814
openSNP	rs63750814
23andMe	rs63750814
SNPshot	rs63750814
SNPdbe	rs63750814
MSV3d	rs63750814
GWAS Ctlg	rs63750814

Max Magnitude

6

ClinVar
Risk	rs63750814(A;A)
Alt	rs63750814(A;A)
Reference	Rs63750814(-;-)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37059066dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075892.2, RCV000486051.1,