rs797045856

Merged into

rs113994201

Orientation

plus

Stabilized

plus

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

Make rs797045856(-;G)

Make rs797045856(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

2680206

Gene

PAFAH1B1

is a	snp
is	mentioned by
dbSNP	rs797045856
dbSNP (classic)	rs797045856
ClinGen	rs797045856
ebi	rs797045856
HLI	rs797045856
Exac	rs797045856
Gnomad	rs797045856
Varsome	rs797045856
LitVar	rs797045856
Map	rs797045856
PheGenI	rs797045856
Biobank	rs797045856
1000 genomes	rs797045856
hgdp	rs797045856
ensembl	rs797045856
geneview	rs797045856
scholar	rs797045856
google	rs797045856
pharmgkb	rs797045856
gwascentral	rs797045856
openSNP	rs797045856
23andMe	rs797045856
SNPshot	rs797045856
SNPdbe	rs797045856
MSV3d	rs797045856
GWAS Ctlg	rs797045856

Status

Merged into rs113994201

Max Magnitude

0

ClinVar
Risk	rs797045856(G;G)
Alt	rs797045856(G;G)
Reference	Rs797045856(;)
Significance	Pathogenic
Disease	Lissencephaly 1
Variation	info
Gene	PAFAH1B1
CLNDBN	Lissencephaly 1
Reversed	0
HGVS	NC_000017.10:g.2583505dupG
CLNSRC
CLNACC	RCV000020299.3,