rs587777881

Orientation

minus

Stabilized

minus

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

Make rs587777881(C;C)

Make rs587777881(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

24955509

Gene	MIR6841, NEFL

is a	snp
is	mentioned by
dbSNP	rs587777881
dbSNP (classic)	rs587777881
ClinGen	rs587777881
ebi	rs587777881
HLI	rs587777881
Exac	rs587777881
Gnomad	rs587777881
Varsome	rs587777881
LitVar	rs587777881
Map	rs587777881
PheGenI	rs587777881
Biobank	rs587777881
1000 genomes	rs587777881
hgdp	rs587777881
ensembl	rs587777881
geneview	rs587777881
scholar	rs587777881
google	rs587777881
pharmgkb	rs587777881
gwascentral	rs587777881
openSNP	rs587777881
23andMe	rs587777881
SNPshot	rs587777881
SNPdbe	rs587777881
MSV3d	rs587777881
GWAS Ctlg	rs587777881

Max Magnitude

0

ClinVar
Risk	rs587777881(C;C)
Alt	rs587777881(C;C)
Reference	Rs587777881(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MIR6841 NEFL
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.24813023A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000143807.1,