rs763711252

Orientation

plus

Stabilized

plus

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

Make rs763711252(A;G)

Make rs763711252(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

102000305

Gene

DYNC1H1

is a	snp
is	mentioned by
dbSNP	rs763711252
dbSNP (classic)	rs763711252
ClinGen	rs763711252
ebi	rs763711252
HLI	rs763711252
Exac	rs763711252
Gnomad	rs763711252
Varsome	rs763711252
LitVar	rs763711252
Map	rs763711252
PheGenI	rs763711252
Biobank	rs763711252
1000 genomes	rs763711252
hgdp	rs763711252
ensembl	rs763711252
geneview	rs763711252
scholar	rs763711252
google	rs763711252
pharmgkb	rs763711252
gwascentral	rs763711252
openSNP	rs763711252
23andMe	rs763711252
SNPshot	rs763711252
SNPdbe	rs763711252
MSV3d	rs763711252
GWAS Ctlg	rs763711252

Max Magnitude

0

ClinVar
Risk	rs763711252(C;C) rs763711252(G;G)
Alt	rs763711252(C;C) rs763711252(G;G)
Reference	Rs763711252(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYNC1H1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.102466642A>C
CLNSRC
CLNACC	RCV000484802.1,