Original source

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

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

Chromosome 8:127401060 (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.127401060G>T
ENST00000502082.3:n.1176+19769C>A
ENST00000501396.3:n.546+19769C>A
ENST00000523825.1:n.546+19769C>A

This variation has assays on 13 chips - click the plus to show

Variation displays