rs587777049

Orientation

plus

Stabilized

minus

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

Make rs587777049(G;T)

Make rs587777049(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

27862558

Gene

ARMC4

is a	snp
is	mentioned by
dbSNP	rs587777049
dbSNP (classic)	rs587777049
ClinGen	rs587777049
ebi	rs587777049
HLI	rs587777049
Exac	rs587777049
Gnomad	rs587777049
Varsome	rs587777049
LitVar	rs587777049
Map	rs587777049
PheGenI	rs587777049
Biobank	rs587777049
1000 genomes	rs587777049
hgdp	rs587777049
ensembl	rs587777049
geneview	rs587777049
scholar	rs587777049
google	rs587777049
pharmgkb	rs587777049
gwascentral	rs587777049
openSNP	rs587777049
23andMe	rs587777049
SNPshot	rs587777049
SNPdbe	rs587777049
MSV3d	rs587777049
GWAS Ctlg	rs587777049

Max Magnitude

0

ClinVar
Risk	Rs587777049(G;G) rs587777049(T;T)
Alt	Rs587777049(G;G) rs587777049(T;T)
Reference	Rs587777049(C;C)
Significance	Pathogenic
Disease	Primary ciliary dyskinesia 23
Variation	info
Gene	ARMC4
CLNDBN	Primary ciliary dyskinesia 23
Reversed	1
HGVS	NC_000010.10:g.28151487G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000056286.4,