rs104893679

Orientation

plus

Stabilized

plus

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

Make rs104893679(C;C)

Make rs104893679(C;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

97791797

Gene

ARL6

is a	snp
is	mentioned by
dbSNP	rs104893679
dbSNP (classic)	rs104893679
ClinGen	rs104893679
ebi	rs104893679
HLI	rs104893679
Exac	rs104893679
Gnomad	rs104893679
Varsome	rs104893679
LitVar	rs104893679
Map	rs104893679
PheGenI	rs104893679
Biobank	rs104893679
1000 genomes	rs104893679
hgdp	rs104893679
ensembl	rs104893679
geneview	rs104893679
scholar	rs104893679
google	rs104893679
pharmgkb	rs104893679
gwascentral	rs104893679
openSNP	rs104893679
23andMe	rs104893679
SNPshot	rs104893679
SNPdbe	rs104893679
MSV3d	rs104893679
GWAS Ctlg	rs104893679

Max Magnitude

0

OMIM	608845
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104893679(C;C)
Alt	rs104893679(C;C)
Reference	Rs104893679(G;G)
Significance	Other
Disease	Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 1
Variation	info
Gene	ARL6 LOC101929298
CLNDBN	Bardet-Biedl syndrome 3 Bardet-Biedl syndrome 1, modifier of
Reversed	0
HGVS	NC_000003.11:g.97510641G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002121.3, RCV000002122.4,