rs879253956

Orientation

plus

Stabilized

plus

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

Make rs879253956(C;T)

Make rs879253956(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

14

Position

102027662

Gene

DYNC1H1

is a	snp
is	mentioned by
dbSNP	rs879253956
dbSNP (classic)	rs879253956
ClinGen	rs879253956
ebi	rs879253956
HLI	rs879253956
Exac	rs879253956
Gnomad	rs879253956
Varsome	rs879253956
LitVar	rs879253956
Map	rs879253956
PheGenI	rs879253956
Biobank	rs879253956
1000 genomes	rs879253956
hgdp	rs879253956
ensembl	rs879253956
geneview	rs879253956
scholar	rs879253956
google	rs879253956
pharmgkb	rs879253956
gwascentral	rs879253956
openSNP	rs879253956
23andMe	rs879253956
SNPshot	rs879253956
SNPdbe	rs879253956
MSV3d	rs879253956
GWAS Ctlg	rs879253956

Max Magnitude

0

ClinVar
Risk	rs879253956(T;T)
Alt	rs879253956(T;T)
Reference	Rs879253956(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DYNC1H1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.102493999C>T
CLNSRC
CLNACC	RCV000236549.2,