rs387907132

Orientation

plus

Stabilized

plus

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

Make rs387907132(A;G)

Make rs387907132(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

61366203

Gene

TMEM138

is a	snp
is	mentioned by
dbSNP	rs387907132
dbSNP (classic)	rs387907132
ClinGen	rs387907132
ebi	rs387907132
HLI	rs387907132
Exac	rs387907132
Gnomad	rs387907132
Varsome	rs387907132
LitVar	rs387907132
Map	rs387907132
PheGenI	rs387907132
Biobank	rs387907132
1000 genomes	rs387907132
hgdp	rs387907132
ensembl	rs387907132
geneview	rs387907132
scholar	rs387907132
google	rs387907132
pharmgkb	rs387907132
gwascentral	rs387907132
openSNP	rs387907132
23andMe	rs387907132
SNPshot	rs387907132
SNPdbe	rs387907132
MSV3d	rs387907132
GWAS Ctlg	rs387907132

Max Magnitude

0

ClinVar
Risk	rs387907132(G;G)
Alt	rs387907132(G;G)
Reference	Rs387907132(A;A)
Significance	Pathogenic
Disease	Joubert syndrome 16 not provided
Variation	info
Gene	TMEM138
CLNDBN	Joubert syndrome 16 not provided
Reversed	0
HGVS	NC_000011.9:g.61133675A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000024187.2, RCV000423402.1,