rs63750781

Orientation

plus

Stabilized

plus

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

Make rs63750781(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004444

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750781
dbSNP (classic)	rs63750781
ClinGen	rs63750781
ebi	rs63750781
HLI	rs63750781
Exac	rs63750781
Gnomad	rs63750781
Varsome	rs63750781
LitVar	rs63750781
Map	rs63750781
PheGenI	rs63750781
Biobank	rs63750781
1000 genomes	rs63750781
hgdp	rs63750781
ensembl	rs63750781
geneview	rs63750781
scholar	rs63750781
google	rs63750781
pharmgkb	rs63750781
gwascentral	rs63750781
openSNP	rs63750781
23andMe	rs63750781
SNPshot	rs63750781
SNPdbe	rs63750781
MSV3d	rs63750781
GWAS Ctlg	rs63750781

Merged from

Rs121912961

Max Magnitude

6

ClinVar
Risk	rs63750781(G;G) rs63750781(T;T)
Alt	rs63750781(G;G) rs63750781(T;T)
Reference	Rs63750781(C;C)
Significance	Other
Disease	Lynch syndrome not provided Lynch syndrome II Lynch syndrome I
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided Lynch syndrome II Lynch syndrome I
Reversed	0
HGVS	NC_000003.11:g.37045935C>G; NC_000003.11:g.37045935C>T
CLNSRC	UniProtKB (protein) OMIM Allelic Variant
CLNACC	RCV000075665.2, RCV000202256.1, RCV000018626.23, RCV000075666.5, RCV000144599.1, RCV000160518.3,