rs63751701

Orientation

plus

Stabilized

plus

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

Make rs63751701(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993663

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs63751701
dbSNP (classic)	rs63751701
ClinGen	rs63751701
ebi	rs63751701
HLI	rs63751701
Exac	rs63751701
Gnomad	rs63751701
Varsome	rs63751701
LitVar	rs63751701
Map	rs63751701
PheGenI	rs63751701
Biobank	rs63751701
1000 genomes	rs63751701
hgdp	rs63751701
ensembl	rs63751701
geneview	rs63751701
scholar	rs63751701
google	rs63751701
pharmgkb	rs63751701
gwascentral	rs63751701
openSNP	rs63751701
23andMe	rs63751701
SNPshot	rs63751701
SNPdbe	rs63751701
MSV3d	rs63751701
GWAS Ctlg	rs63751701

Max Magnitude

6

ClinVar
Risk	rs63751701(A;A) rs63751701(T;T)
Alt	rs63751701(A;A) rs63751701(T;T)
Reference	Rs63751701(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37035154G>A; NC_000003.11:g.37035154G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075134.2, RCV000202285.1, RCV000075135.2,