Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.44 (T)
Location

Chromosome 8:128413305 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR078267

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17467153, rs61163584

This variation has 4 HGVS names - click the plus to show

8:g.128413305G>T
ENST00000502082.1:n.1176+19769C>A
ENST00000501396.1:n.546+19769C>A
ENST00000523825.1:n.546+19769C>A

This variation has assays on 12 chips - click the plus to show

Variation displays