rs41298896

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;G)	0	Benign variant according to ClinVar
(G;G)	0	common in clinvar

Make rs41298896(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

14926856

Gene

DCLRE1C

is a	snp
is	mentioned by
dbSNP	rs41298896
dbSNP (classic)	rs41298896
ClinGen	rs41298896
ebi	rs41298896
HLI	rs41298896
Exac	rs41298896
Gnomad	rs41298896
Varsome	rs41298896
LitVar	rs41298896
Map	rs41298896
PheGenI	rs41298896
Biobank	rs41298896
1000 genomes	rs41298896
hgdp	rs41298896
ensembl	rs41298896
geneview	rs41298896
scholar	rs41298896
google	rs41298896
pharmgkb	rs41298896
gwascentral	rs41298896
openSNP	rs41298896
23andMe	rs41298896
SNPshot	rs41298896
SNPdbe	rs41298896
MSV3d	rs41298896
GWAS Ctlg	rs41298896

Max Magnitude

0

ClinVar
Risk	rs41298896(C;C)
Alt	rs41298896(C;C)
Reference	Rs41298896(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified Histiocytic medullary reticulosis
Variation	info
Gene	DCLRE1C
CLNDBN	not provided not specified Histiocytic medullary reticulosis
Reversed	0
HGVS	NC_000010.10:g.14968855G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000124664.3, RCV000212484.1, RCV000348357.1,