rs606231276

Orientation

minus

Stabilized

minus

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

Make rs606231276(C;C)

Make rs606231276(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43238827

Gene

TGM5

is a	snp
is	mentioned by
dbSNP	rs606231276
dbSNP (classic)	rs606231276
ClinGen	rs606231276
ebi	rs606231276
HLI	rs606231276
Exac	rs606231276
Gnomad	rs606231276
Varsome	rs606231276
LitVar	rs606231276
Map	rs606231276
PheGenI	rs606231276
Biobank	rs606231276
1000 genomes	rs606231276
hgdp	rs606231276
ensembl	rs606231276
geneview	rs606231276
scholar	rs606231276
google	rs606231276
pharmgkb	rs606231276
gwascentral	rs606231276
openSNP	rs606231276
23andMe	rs606231276
SNPshot	rs606231276
SNPdbe	rs606231276
MSV3d	rs606231276
GWAS Ctlg	rs606231276

Max Magnitude

0

ClinVar
Risk	rs606231276(C;C)
Alt	rs606231276(C;C)
Reference	Rs606231276(G;G)
Significance	Pathogenic
Disease	Peeling skin syndrome
Variation	info
Gene	TGM5
CLNDBN	Peeling skin syndrome, acral type
Reversed	1
HGVS	NC_000015.9:g.43531025C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144911.4,