rs137853234

Orientation

plus

Stabilized

plus

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

Make rs137853234(C;C)

Make rs137853234(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

72060463

Gene	HP, TXNL4B

is a	snp
is	mentioned by
dbSNP	rs137853234
dbSNP (classic)	rs137853234
ClinGen	rs137853234
ebi	rs137853234
HLI	rs137853234
Exac	rs137853234
Gnomad	rs137853234
Varsome	rs137853234
LitVar	rs137853234
Map	rs137853234
PheGenI	rs137853234
Biobank	rs137853234
1000 genomes	rs137853234
hgdp	rs137853234
ensembl	rs137853234
geneview	rs137853234
scholar	rs137853234
google	rs137853234
pharmgkb	rs137853234
gwascentral	rs137853234
openSNP	rs137853234
23andMe	rs137853234
SNPshot	rs137853234
SNPdbe	rs137853234
MSV3d	rs137853234
GWAS Ctlg	rs137853234

Max Magnitude

0

OMIM	140100
Desc
Variant	0005
Related	also

ClinVar
Risk	rs137853234(C;C)
Alt	rs137853234(C;C)
Reference	Rs137853234(T;T)
Significance	Untested
Disease	Anhaptoglobinemia
Variation	info
Gene	HP
CLNDBN	Anhaptoglobinemia
Reversed	0
HGVS	NC_000016.9:g.72094362T>C
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000037521.1, SCV000037521.1,