rs62636502

Orientation

minus

Stabilized

minus

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

Make rs62636502(C;C)

Make rs62636502(C;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

24955713

Gene	MIR6841, NEFL

is a	snp
is	mentioned by
dbSNP	rs62636502
dbSNP (classic)	rs62636502
ClinGen	rs62636502
ebi	rs62636502
HLI	rs62636502
Exac	rs62636502
Gnomad	rs62636502
Varsome	rs62636502
LitVar	rs62636502
Map	rs62636502
PheGenI	rs62636502
Biobank	rs62636502
1000 genomes	rs62636502
hgdp	rs62636502
ensembl	rs62636502
geneview	rs62636502
scholar	rs62636502
google	rs62636502
pharmgkb	rs62636502
gwascentral	rs62636502
openSNP	rs62636502
23andMe	rs62636502
SNPshot	rs62636502
SNPdbe	rs62636502
MSV3d	rs62636502
GWAS Ctlg	rs62636502

Max Magnitude

0

ClinVar
Risk	rs62636502(C;C) rs62636502(G;G)
Alt	rs62636502(C;C) rs62636502(G;G)
Reference	Rs62636502(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MIR6841 NEFL
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.24813227A>C; NC_000008.10:g.24813227A>G
CLNSRC	ClinVar Epithelial Biology
CLNACC	RCV000143811.1, RCV000057148.1,