rs63751465

Orientation

plus

Stabilized

plus

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

Make rs63751465(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996696

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751465
dbSNP (classic)	rs63751465
ClinGen	rs63751465
ebi	rs63751465
HLI	rs63751465
Exac	rs63751465
Gnomad	rs63751465
Varsome	rs63751465
LitVar	rs63751465
Map	rs63751465
PheGenI	rs63751465
Biobank	rs63751465
1000 genomes	rs63751465
hgdp	rs63751465
ensembl	rs63751465
geneview	rs63751465
scholar	rs63751465
google	rs63751465
pharmgkb	rs63751465
gwascentral	rs63751465
openSNP	rs63751465
23andMe	rs63751465
SNPshot	rs63751465
SNPdbe	rs63751465
MSV3d	rs63751465
GWAS Ctlg	rs63751465

Max Magnitude

6

ClinVar
Risk	rs63751465(A;A) rs63751465(T;T)
Alt	rs63751465(A;A) rs63751465(T;T)
Reference	Rs63751465(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not specified
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not specified
Reversed	0
HGVS	NC_000003.11:g.37038187G>A; NC_000003.11:g.37038187G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075435.2, RCV000202218.1, RCV000469604.1,