Original source

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

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

Chromosome 1:110152730 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021611

Most severe consequence
Clinical significance

Synonyms

LSDB 2414

This variation has 3 HGVS names - click the plus to show

1:g.110152730G>A
ENST00000351050.3:c.235C>T
ENSP00000251337.3:p.Gln79Ter

Variation displays