rs886039401

Orientation

minus

Stabilized

minus

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

Make rs886039401(A;A)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

92226525

Gene

KRIT1

is a	snp
is	mentioned by
dbSNP	rs886039401
dbSNP (classic)	rs886039401
ClinGen	rs886039401
ebi	rs886039401
HLI	rs886039401
Exac	rs886039401
Gnomad	rs886039401
Varsome	rs886039401
LitVar	rs886039401
Map	rs886039401
PheGenI	rs886039401
Biobank	rs886039401
1000 genomes	rs886039401
hgdp	rs886039401
ensembl	rs886039401
geneview	rs886039401
scholar	rs886039401
google	rs886039401
pharmgkb	rs886039401
gwascentral	rs886039401
openSNP	rs886039401
23andMe	rs886039401
SNPshot	rs886039401
SNPdbe	rs886039401
MSV3d	rs886039401
GWAS Ctlg	rs886039401

Max Magnitude

0

aka c.1146+1G>A

ClinVar
Risk	rs886039401(A;A)
Alt	rs886039401(A;A)
Reference	Rs886039401(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRIT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.91855839C>T
CLNSRC
CLNACC	RCV000254945.1,