rs63751219

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;TA)	6	Lynch syndrome, pathogenic mutation
(I;I)	0

Make rs63751219(TA;TA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429793

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751219
dbSNP (classic)	rs63751219
ClinGen	rs63751219
ebi	rs63751219
HLI	rs63751219
Exac	rs63751219
Gnomad	rs63751219
Varsome	rs63751219
LitVar	rs63751219
Map	rs63751219
PheGenI	rs63751219
Biobank	rs63751219
1000 genomes	rs63751219
hgdp	rs63751219
ensembl	rs63751219
geneview	rs63751219
scholar	rs63751219
google	rs63751219
pharmgkb	rs63751219
gwascentral	rs63751219
openSNP	rs63751219
23andMe	rs63751219
SNPshot	rs63751219
SNPdbe	rs63751219
MSV3d	rs63751219
GWAS Ctlg	rs63751219

Max Magnitude

6

ClinVar
Risk	rs63751219(TA;TA)
Alt	rs63751219(TA;TA)
Reference	Rs63751219(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656931_47656932dupTA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076044.2,