rs200019422

Orientation

plus

Stabilized

plus

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

Make rs200019422(A;A)

Make rs200019422(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

49447669

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs200019422
dbSNP (classic)	rs200019422
ClinGen	rs200019422
ebi	rs200019422
HLI	rs200019422
Exac	rs200019422
Gnomad	rs200019422
Varsome	rs200019422
LitVar	rs200019422
Map	rs200019422
PheGenI	rs200019422
Biobank	rs200019422
1000 genomes	rs200019422
hgdp	rs200019422
ensembl	rs200019422
geneview	rs200019422
scholar	rs200019422
google	rs200019422
pharmgkb	rs200019422
gwascentral	rs200019422
openSNP	rs200019422
23andMe	rs200019422
SNPshot	rs200019422
SNPdbe	rs200019422
MSV3d	rs200019422
GWAS Ctlg	rs200019422

Max Magnitude

0

ClinVar
Risk	rs200019422(A;A)
Alt	rs200019422(A;A)
Reference	Rs200019422(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MUT
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.49415382C>A
CLNSRC
CLNACC	RCV000186049.1,