rs63749868

Orientation

plus

Stabilized

plus

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

Make rs63749868(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047559

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749868
dbSNP (classic)	rs63749868
ClinGen	rs63749868
ebi	rs63749868
HLI	rs63749868
Exac	rs63749868
Gnomad	rs63749868
Varsome	rs63749868
LitVar	rs63749868
Map	rs63749868
PheGenI	rs63749868
Biobank	rs63749868
1000 genomes	rs63749868
hgdp	rs63749868
ensembl	rs63749868
geneview	rs63749868
scholar	rs63749868
google	rs63749868
pharmgkb	rs63749868
gwascentral	rs63749868
openSNP	rs63749868
23andMe	rs63749868
SNPshot	rs63749868
SNPdbe	rs63749868
MSV3d	rs63749868
GWAS Ctlg	rs63749868

Max Magnitude

6

ClinVar
Risk	rs63749868(-;-) Rs63749868(TAGA;TAGA)
Alt	rs63749868(-;-) Rs63749868(TAGA;TAGA)
Reference	Rs63749868(ATAG;ATAG)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37089050_37089053delATAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075362.2, RCV000202011.1,