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 1:173881080 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910056

Most severe consequence
Clinical significance

Synonyms

LSDB 365

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

1:g.173881080G>A
ENST00000367698.3:c.481C>T
ENSP00000356671.3:p.Arg161Ter
ENST00000487183.1:n.186C>T

Variation displays