rs63751682

Orientation

plus

Stabilized

plus

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

Make rs63751682(A;G)

Make rs63751682(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048608

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751682
dbSNP (classic)	rs63751682
ClinGen	rs63751682
ebi	rs63751682
HLI	rs63751682
Exac	rs63751682
Gnomad	rs63751682
Varsome	rs63751682
LitVar	rs63751682
Map	rs63751682
PheGenI	rs63751682
Biobank	rs63751682
1000 genomes	rs63751682
hgdp	rs63751682
ensembl	rs63751682
geneview	rs63751682
scholar	rs63751682
google	rs63751682
pharmgkb	rs63751682
gwascentral	rs63751682
openSNP	rs63751682
23andMe	rs63751682
SNPshot	rs63751682
SNPdbe	rs63751682
MSV3d	rs63751682
GWAS Ctlg	rs63751682

Max Magnitude

6

ClinVar
Risk	rs63751682(C;C) rs63751682(G;G)
Alt	rs63751682(C;C) rs63751682(G;G)
Reference	Rs63751682(A;A)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not specified
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not specified
Reversed	0
HGVS	NC_000003.11:g.37090099A>C; NC_000003.11:g.37090099A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075452.2, RCV000075453.2, RCV000218482.1,