rs797044954

Orientation

minus

Stabilized

minus

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

Make rs797044954(A;A)

Make rs797044954(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

75540155

Gene

TMEM231

is a	snp
is	mentioned by
dbSNP	rs797044954
dbSNP (classic)	rs797044954
ClinGen	rs797044954
ebi	rs797044954
HLI	rs797044954
Exac	rs797044954
Gnomad	rs797044954
Varsome	rs797044954
LitVar	rs797044954
Map	rs797044954
PheGenI	rs797044954
Biobank	rs797044954
1000 genomes	rs797044954
hgdp	rs797044954
ensembl	rs797044954
geneview	rs797044954
scholar	rs797044954
google	rs797044954
pharmgkb	rs797044954
gwascentral	rs797044954
openSNP	rs797044954
23andMe	rs797044954
SNPshot	rs797044954
SNPdbe	rs797044954
MSV3d	rs797044954
GWAS Ctlg	rs797044954

Max Magnitude

0

ClinVar
Risk	rs797044954(A;A)
Alt	rs797044954(A;A)
Reference	Rs797044954(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	TMEM231
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000016.9:g.75574053C>T
CLNSRC
CLNACC	RCV000190811.1,