rs587776685

Orientation

plus

Stabilized

minus

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

Make rs587776685(-;-)

Make rs587776685(-;T)

Reference

GRCh38 38.1/142

Chromosome

13

Position

101726732

Gene

FGF14

is a	snp
is	mentioned by
dbSNP	rs587776685
dbSNP (classic)	rs587776685
ClinGen	rs587776685
ebi	rs587776685
HLI	rs587776685
Exac	rs587776685
Gnomad	rs587776685
Varsome	rs587776685
LitVar	rs587776685
Map	rs587776685
PheGenI	rs587776685
Biobank	rs587776685
1000 genomes	rs587776685
hgdp	rs587776685
ensembl	rs587776685
geneview	rs587776685
scholar	rs587776685
google	rs587776685
pharmgkb	rs587776685
gwascentral	rs587776685
openSNP	rs587776685
23andMe	rs587776685
SNPshot	rs587776685
SNPdbe	rs587776685
MSV3d	rs587776685
GWAS Ctlg	rs587776685

Max Magnitude

0

ClinVar
Risk	Rs587776685(T;T) rs587776685(-;-)
Alt	Rs587776685(T;T) rs587776685(-;-)
Reference	Rs587776685(A;A)
Significance	Pathogenic
Disease	Spinocerebellar ataxia 27
Variation	info
Gene	FGF14
CLNDBN	Spinocerebellar ataxia 27
Reversed	1
HGVS	NC_000013.10:g.102379082delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008585.3,