rs587784261

Orientation

plus

Stabilized

plus

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

Make rs587784261(A;A)

Make rs587784261(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

2667170

Gene

PAFAH1B1

is a	snp
is	mentioned by
dbSNP	rs587784261
dbSNP (classic)	rs587784261
ClinGen	rs587784261
ebi	rs587784261
HLI	rs587784261
Exac	rs587784261
Gnomad	rs587784261
Varsome	rs587784261
LitVar	rs587784261
Map	rs587784261
PheGenI	rs587784261
Biobank	rs587784261
1000 genomes	rs587784261
hgdp	rs587784261
ensembl	rs587784261
geneview	rs587784261
scholar	rs587784261
google	rs587784261
pharmgkb	rs587784261
gwascentral	rs587784261
openSNP	rs587784261
23andMe	rs587784261
SNPshot	rs587784261
SNPdbe	rs587784261
MSV3d	rs587784261
GWAS Ctlg	rs587784261

Max Magnitude

0

ClinVar
Risk	rs587784261(A;A)
Alt	rs587784261(A;A)
Reference	Rs587784261(T;T)
Significance	Pathogenic
Disease	Lissencephaly 1
Variation	info
Gene	PAFAH1B1
CLNDBN	Lissencephaly 1
Reversed	0
HGVS	NC_000017.10:g.2570464T>A
CLNSRC
CLNACC	RCV000147031.1,