Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.14 (C)
Location

Chromosome 10:81889983 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59962958

HGVS names

This variant has 8 HGVS names - Hide

10:g.81889983T>C
ENST00000602794.5:c.*371+318T>C
ENST00000555784.5:c.135+11888T>C
ENST00000404576.6:c.135+11888T>C
ENST00000404547.5:c.823+13820T>C
ENST00000556918.5:c.135+11888T>C
ENST00000372142.6:c.60+11963T>C
ENST00000372141.6:c.823+13820T>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3766 sample genotypes and is mentioned in 3 citations.

Variant displays