rs63750714

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;C)	5	Unclear significance; possible Lynch syndrome mutation
(C;C)	0	common/normal

Make rs63750714(-;-)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47803442

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750714
dbSNP (classic)	rs63750714
ClinGen	rs63750714
ebi	rs63750714
HLI	rs63750714
Exac	rs63750714
Gnomad	rs63750714
Varsome	rs63750714
LitVar	rs63750714
Map	rs63750714
PheGenI	rs63750714
Biobank	rs63750714
1000 genomes	rs63750714
hgdp	rs63750714
ensembl	rs63750714
geneview	rs63750714
scholar	rs63750714
google	rs63750714
pharmgkb	rs63750714
gwascentral	rs63750714
openSNP	rs63750714
23andMe	rs63750714
SNPshot	rs63750714
SNPdbe	rs63750714
MSV3d	rs63750714
GWAS Ctlg	rs63750714

Max Magnitude

5

c.3195delC

23andMe name: i5901028