rs1043384862

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

103165911

Gene

DYNC2H1

is a	snp
is	mentioned by
dbSNP	rs1043384862
dbSNP (classic)	rs1043384862
ClinGen	rs1043384862
ebi	rs1043384862
HLI	rs1043384862
Exac	rs1043384862
Gnomad	rs1043384862
Varsome	rs1043384862
LitVar	rs1043384862
Map	rs1043384862
PheGenI	rs1043384862
Biobank	rs1043384862
1000 genomes	rs1043384862
hgdp	rs1043384862
ensembl	rs1043384862
geneview	rs1043384862
scholar	rs1043384862
google	rs1043384862
pharmgkb	rs1043384862
gwascentral	rs1043384862
openSNP	rs1043384862
23andMe	rs1043384862
SNPshot	rs1043384862
SNPdbe	rs1043384862
MSV3d	rs1043384862
GWAS Ctlg	rs1043384862

Max Magnitude

0

ClinVar
Risk	rs1043384862(T;T)
Alt	rs1043384862(T;T)
Reference	Rs1043384862(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYNC2H1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.103036640C>T
CLNSRC
CLNACC	RCV000413597.1,