rs137852736

Orientation

minus

Stabilized

minus

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

Make rs137852736(-;-)

Make rs137852736(-;TC)

Reference

GRCh38 38.1/141

Chromosome

5

Position

16616953

Gene	FAM134B, LOC101929524

is a	snp
is	mentioned by
dbSNP	rs137852736
dbSNP (classic)	rs137852736
ClinGen	rs137852736
ebi	rs137852736
HLI	rs137852736
Exac	rs137852736
Gnomad	rs137852736
Varsome	rs137852736
LitVar	rs137852736
Map	rs137852736
PheGenI	rs137852736
Biobank	rs137852736
1000 genomes	rs137852736
hgdp	rs137852736
ensembl	rs137852736
geneview	rs137852736
scholar	rs137852736
google	rs137852736
pharmgkb	rs137852736
gwascentral	rs137852736
openSNP	rs137852736
23andMe	rs137852736
SNPshot	rs137852736
SNPdbe	rs137852736
MSV3d	rs137852736
GWAS Ctlg	rs137852736

Max Magnitude

0

ClinVar
Risk	rs137852736(-;-)
Alt	rs137852736(-;-)
Reference	Rs137852736(TC;TC)
Significance	Pathogenic
Disease	Hereditary sensory and autonomic neuropathy type IIA
Variation	info
Gene	FAM134B LOC101929524
CLNDBN	Hereditary sensory and autonomic neuropathy type IIA
Reversed	1
HGVS	NC_000005.9:g.16617062_16617063delGA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020419.1,

OMIM	201300
Desc
Variant
Related	also