rs63751639

Orientation

plus

Stabilized

plus

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

Make rs63751639(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047671

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751639
dbSNP (classic)	rs63751639
ClinGen	rs63751639
ebi	rs63751639
HLI	rs63751639
Exac	rs63751639
Gnomad	rs63751639
Varsome	rs63751639
LitVar	rs63751639
Map	rs63751639
PheGenI	rs63751639
Biobank	rs63751639
1000 genomes	rs63751639
hgdp	rs63751639
ensembl	rs63751639
geneview	rs63751639
scholar	rs63751639
google	rs63751639
pharmgkb	rs63751639
gwascentral	rs63751639
openSNP	rs63751639
23andMe	rs63751639
SNPshot	rs63751639
SNPdbe	rs63751639
MSV3d	rs63751639
GWAS Ctlg	rs63751639

Max Magnitude

6

ClinVar
Risk	rs63751639(-;-)
Alt	rs63751639(-;-)
Reference	Rs63751639(GGAAA;GGAAA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089162_37089166delGGAAA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075401.2,