rs104893681

Orientation

plus

Stabilized

plus

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

Make rs104893681(G;G)

Make rs104893681(G;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

97791800

Gene

ARL6

is a	snp
is	mentioned by
dbSNP	rs104893681
dbSNP (classic)	rs104893681
ClinGen	rs104893681
ebi	rs104893681
HLI	rs104893681
Exac	rs104893681
Gnomad	rs104893681
Varsome	rs104893681
LitVar	rs104893681
Map	rs104893681
PheGenI	rs104893681
Biobank	rs104893681
1000 genomes	rs104893681
hgdp	rs104893681
ensembl	rs104893681
geneview	rs104893681
scholar	rs104893681
google	rs104893681
pharmgkb	rs104893681
gwascentral	rs104893681
openSNP	rs104893681
23andMe	rs104893681
SNPshot	rs104893681
SNPdbe	rs104893681
MSV3d	rs104893681
GWAS Ctlg	rs104893681

Max Magnitude

0

OMIM	608845
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104893681(G;G)
Alt	rs104893681(G;G)
Reference	Rs104893681(T;T)
Significance	Pathogenic
Disease	Bardet-Biedl syndrome 3
Variation	info
Gene	ARL6 LOC101929298
CLNDBN	Bardet-Biedl syndrome 3
Reversed	0
HGVS	NC_000003.11:g.97510644T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002124.3,