Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:173881079 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900039

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 366

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

1:g.173881079C>T
ENST00000487183.1:n.187G>A
ENST00000367698.3:c.482G>A
ENSP00000356671.3:p.Arg161Gln

Variation displays