rs1064797348

Orientation

plus

Stabilized

plus

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

Chromosome

8

Position

101573734

Gene

GRHL2

is a	snp
is	mentioned by
dbSNP	rs1064797348
dbSNP (classic)	rs1064797348
ClinGen	rs1064797348
ebi	rs1064797348
HLI	rs1064797348
Exac	rs1064797348
Gnomad	rs1064797348
Varsome	rs1064797348
LitVar	rs1064797348
Map	rs1064797348
PheGenI	rs1064797348
Biobank	rs1064797348
1000 genomes	rs1064797348
hgdp	rs1064797348
ensembl	rs1064797348
geneview	rs1064797348
scholar	rs1064797348
google	rs1064797348
pharmgkb	rs1064797348
gwascentral	rs1064797348
openSNP	rs1064797348
23andMe	rs1064797348
SNPshot	rs1064797348
SNPdbe	rs1064797348
MSV3d	rs1064797348
GWAS Ctlg	rs1064797348

Max Magnitude

0

ClinVar
Risk	rs1064797348(-;-)
Alt	rs1064797348(-;-)
Reference	Rs1064797348(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRHL2
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.102585962delG
CLNSRC
CLNACC	RCV000487664.1,