rs63750211

Orientation

plus

Stabilized

plus

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

Make rs63750211(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37008904

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750211
dbSNP (classic)	rs63750211
ClinGen	rs63750211
ebi	rs63750211
HLI	rs63750211
Exac	rs63750211
Gnomad	rs63750211
Varsome	rs63750211
LitVar	rs63750211
Map	rs63750211
PheGenI	rs63750211
Biobank	rs63750211
1000 genomes	rs63750211
hgdp	rs63750211
ensembl	rs63750211
geneview	rs63750211
scholar	rs63750211
google	rs63750211
pharmgkb	rs63750211
gwascentral	rs63750211
openSNP	rs63750211
23andMe	rs63750211
SNPshot	rs63750211
SNPdbe	rs63750211
MSV3d	rs63750211
GWAS Ctlg	rs63750211

Max Magnitude

6

ClinVar
Risk	rs63750211(G;G)
Alt	rs63750211(G;G)
Reference	Rs63750211(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37050395A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075747.3,