rs137854907

Orientation

plus

Stabilized

plus

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

Make rs137854907(C;C)

Make rs137854907(C;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

97784972

Gene

ARL6

is a	snp
is	mentioned by
dbSNP	rs137854907
dbSNP (classic)	rs137854907
ClinGen	rs137854907
ebi	rs137854907
HLI	rs137854907
Exac	rs137854907
Gnomad	rs137854907
Varsome	rs137854907
LitVar	rs137854907
Map	rs137854907
PheGenI	rs137854907
Biobank	rs137854907
1000 genomes	rs137854907
hgdp	rs137854907
ensembl	rs137854907
geneview	rs137854907
scholar	rs137854907
google	rs137854907
pharmgkb	rs137854907
gwascentral	rs137854907
openSNP	rs137854907
23andMe	rs137854907
SNPshot	rs137854907
SNPdbe	rs137854907
MSV3d	rs137854907
GWAS Ctlg	rs137854907

Max Magnitude

0

ClinVar
Risk	rs137854907(C;C)
Alt	rs137854907(C;C)
Reference	Rs137854907(T;T)
Significance	Pathogenic
Disease	Bardet-Biedl syndrome
Variation	info
Gene	ARL6 LOC101929298
CLNDBN	Bardet-Biedl syndrome
Reversed	0
HGVS	NC_000003.11:g.97503816T>C
CLNSRC	ClinVar
CLNACC	RCV000058868.1,