rs587777882

Orientation

minus

Stabilized

minus

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

Make rs587777882(C;T)

Make rs587777882(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

24953646

Gene	MIR6841, NEFL

is a	snp
is	mentioned by
dbSNP	rs587777882
dbSNP (classic)	rs587777882
ClinGen	rs587777882
ebi	rs587777882
HLI	rs587777882
Exac	rs587777882
Gnomad	rs587777882
Varsome	rs587777882
LitVar	rs587777882
Map	rs587777882
PheGenI	rs587777882
Biobank	rs587777882
1000 genomes	rs587777882
hgdp	rs587777882
ensembl	rs587777882
geneview	rs587777882
scholar	rs587777882
google	rs587777882
pharmgkb	rs587777882
gwascentral	rs587777882
openSNP	rs587777882
23andMe	rs587777882
SNPshot	rs587777882
SNPdbe	rs587777882
MSV3d	rs587777882
GWAS Ctlg	rs587777882

Max Magnitude

0

ClinVar
Risk	rs587777882(T;T)
Alt	rs587777882(T;T)
Reference	Rs587777882(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MIR6841 NEFL
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.24811160G>A
CLNSRC
CLNACC	RCV000143808.1,