Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 13:102868199 (forward strand) | View in location tab

Co-located

with ESP rs28929496 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

13:g.102868199G>A
ENST00000602836.1:c.3896G>A
ENSP00000473384.1:p.Ala1300Thr
ENST00000355739.6:c.2620G>A
ENSP00000347978.4:p.Ala874Thr
ENST00000481099.1:n.740G>A
ENST00000610537.2:c.2617G>A
ENSP00000478667.1:p.Ala873Thr
ENST00000375954.1:c.319G>A
ENSP00000365121.1:p.Ala107Thr
LRG_464:g.27376G>A
LRG_464t1.1:c.2620G>A
LRG_464p1.1:p.Asn879Lys

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays