rs797044918

Orientation

plus

Stabilized

plus

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

Make rs797044918(-;-)

Make rs797044918(-;AAG)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

102029930

Gene

DYNC1H1

is a	snp
is	mentioned by
dbSNP	rs797044918
dbSNP (classic)	rs797044918
ClinGen	rs797044918
ebi	rs797044918
HLI	rs797044918
Exac	rs797044918
Gnomad	rs797044918
Varsome	rs797044918
LitVar	rs797044918
Map	rs797044918
PheGenI	rs797044918
Biobank	rs797044918
1000 genomes	rs797044918
hgdp	rs797044918
ensembl	rs797044918
geneview	rs797044918
scholar	rs797044918
google	rs797044918
pharmgkb	rs797044918
gwascentral	rs797044918
openSNP	rs797044918
23andMe	rs797044918
SNPshot	rs797044918
SNPdbe	rs797044918
MSV3d	rs797044918
GWAS Ctlg	rs797044918

Max Magnitude

0

ClinVar
Risk	rs797044918(-;-)
Alt	rs797044918(-;-)
Reference	Rs797044918(AAG;AAG)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	DYNC1H1
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000014.8:g.102496267_102496269delAAG
CLNSRC
CLNACC	RCV000190753.1,