rs63750305

Orientation

plus

Stabilized

plus

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

Make rs63750305(-;AT)

Make rs63750305(AT;AT)

Reference

GRCh38 38.1/142

Chromosome

3

Position

37025727

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750305
dbSNP (classic)	rs63750305
ClinGen	rs63750305
ebi	rs63750305
HLI	rs63750305
Exac	rs63750305
Gnomad	rs63750305
Varsome	rs63750305
LitVar	rs63750305
Map	rs63750305
PheGenI	rs63750305
Biobank	rs63750305
1000 genomes	rs63750305
hgdp	rs63750305
ensembl	rs63750305
geneview	rs63750305
scholar	rs63750305
google	rs63750305
pharmgkb	rs63750305
gwascentral	rs63750305
openSNP	rs63750305
23andMe	rs63750305
SNPshot	rs63750305
SNPdbe	rs63750305
MSV3d	rs63750305
GWAS Ctlg	rs63750305

Max Magnitude

6

ClinVar
Risk	rs63750305(AT;AT) rs63750305(TA;TA)
Alt	rs63750305(AT;AT) rs63750305(TA;TA)
Reference	Rs63750305(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067217_37067218dupTA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075114.2,