rs148059981

Orientation

plus

Stabilized

plus

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

Make rs148059981(C;T)

Make rs148059981(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

18

Position

49363233

Gene

DYM

is a	snp
is	mentioned by
dbSNP	rs148059981
dbSNP (classic)	rs148059981
ClinGen	rs148059981
ebi	rs148059981
HLI	rs148059981
Exac	rs148059981
Gnomad	rs148059981
Varsome	rs148059981
LitVar	rs148059981
Map	rs148059981
PheGenI	rs148059981
Biobank	rs148059981
1000 genomes	rs148059981
hgdp	rs148059981
ensembl	rs148059981
geneview	rs148059981
scholar	rs148059981
google	rs148059981
pharmgkb	rs148059981
gwascentral	rs148059981
openSNP	rs148059981
23andMe	rs148059981
SNPshot	rs148059981
SNPdbe	rs148059981
MSV3d	rs148059981
GWAS Ctlg	rs148059981

Max Magnitude

0

ClinVar
Risk	rs148059981(T;T)
Alt	rs148059981(T;T)
Reference	Rs148059981(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYM
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.46889603C>T
CLNSRC
CLNACC	RCV000171274.1,