rs760971556

Orientation

plus

Stabilized

plus

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

Make rs760971556(C;G)

Make rs760971556(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

101986052

Gene

DYNC1H1

is a	snp
is	mentioned by
dbSNP	rs760971556
dbSNP (classic)	rs760971556
ClinGen	rs760971556
ebi	rs760971556
HLI	rs760971556
Exac	rs760971556
Gnomad	rs760971556
Varsome	rs760971556
LitVar	rs760971556
Map	rs760971556
PheGenI	rs760971556
Biobank	rs760971556
1000 genomes	rs760971556
hgdp	rs760971556
ensembl	rs760971556
geneview	rs760971556
scholar	rs760971556
google	rs760971556
pharmgkb	rs760971556
gwascentral	rs760971556
openSNP	rs760971556
23andMe	rs760971556
SNPshot	rs760971556
SNPdbe	rs760971556
MSV3d	rs760971556
GWAS Ctlg	rs760971556

Max Magnitude

0

ClinVar
Risk	rs760971556(G;G)
Alt	rs760971556(G;G)
Reference	Rs760971556(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYNC1H1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.102452389C>G
CLNSRC
CLNACC	RCV000427964.1,