rs63750952

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs63750952(A;G)

Make rs63750952(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996693

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750952
dbSNP (classic)	rs63750952
ClinGen	rs63750952
ebi	rs63750952
HLI	rs63750952
Exac	rs63750952
Gnomad	rs63750952
Varsome	rs63750952
LitVar	rs63750952
Map	rs63750952
PheGenI	rs63750952
Biobank	rs63750952
1000 genomes	rs63750952
hgdp	rs63750952
ensembl	rs63750952
geneview	rs63750952
scholar	rs63750952
google	rs63750952
pharmgkb	rs63750952
gwascentral	rs63750952
openSNP	rs63750952
23andMe	rs63750952
SNPshot	rs63750952
SNPdbe	rs63750952
MSV3d	rs63750952
GWAS Ctlg	rs63750952

Max Magnitude

0

ClinVar
Risk	rs63750952(G;G)
Alt	rs63750952(G;G)
Reference	Rs63750952(A;A)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome II Lynch syndrome I
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not specified Hereditary cancer-predisposing syndrome Lynch syndrome II Lynch syndrome I
Reversed	0
HGVS	NC_000003.11:g.37038184A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075426.3, RCV000160536.3, RCV000217492.2, RCV000410882.1, RCV000490571.1,