rs797044928

Orientation

plus

Stabilized

plus

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

Make rs797044928(A;A)

Make rs797044928(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

102032421

Gene

DYNC1H1

is a	snp
is	mentioned by
dbSNP	rs797044928
dbSNP (classic)	rs797044928
ClinGen	rs797044928
ebi	rs797044928
HLI	rs797044928
Exac	rs797044928
Gnomad	rs797044928
Varsome	rs797044928
LitVar	rs797044928
Map	rs797044928
PheGenI	rs797044928
Biobank	rs797044928
1000 genomes	rs797044928
hgdp	rs797044928
ensembl	rs797044928
geneview	rs797044928
scholar	rs797044928
google	rs797044928
pharmgkb	rs797044928
gwascentral	rs797044928
openSNP	rs797044928
23andMe	rs797044928
SNPshot	rs797044928
SNPdbe	rs797044928
MSV3d	rs797044928
GWAS Ctlg	rs797044928

Max Magnitude

0

ClinVar
Risk	rs797044928(A;A)
Alt	rs797044928(A;A)
Reference	Rs797044928(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	DYNC1H1
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000014.8:g.102498758G>A
CLNSRC
CLNACC	RCV000190767.1,