rs113993965

Orientation

plus

Stabilized

plus

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

Make rs113993965(A;A)

Make rs113993965(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

189808465

Gene

TP63

is a	snp
is	mentioned by
dbSNP	rs113993965
dbSNP (classic)	rs113993965
ClinGen	rs113993965
ebi	rs113993965
HLI	rs113993965
Exac	rs113993965
Gnomad	rs113993965
Varsome	rs113993965
LitVar	rs113993965
Map	rs113993965
PheGenI	rs113993965
Biobank	rs113993965
1000 genomes	rs113993965
hgdp	rs113993965
ensembl	rs113993965
geneview	rs113993965
scholar	rs113993965
google	rs113993965
pharmgkb	rs113993965
gwascentral	rs113993965
openSNP	rs113993965
23andMe	rs113993965
SNPshot	rs113993965
SNPdbe	rs113993965
MSV3d	rs113993965
GWAS Ctlg	rs113993965

Max Magnitude

0

ClinVar
Risk	rs113993965(A;A)
Alt	rs113993965(A;A)
Reference	Rs113993965(G;G)
Significance	Pathogenic
Disease	ADULT syndrome not provided
Variation	info
Gene	TP63
CLNDBN	ADULT syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.189526254G>A; NC_000003.11:g.189526254G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032229.1, RCV000494181.1,