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
Location

Chromosome 7:30969116 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960736

Most severe consequence
Clinical significance

Synonyms

LSDB 2341

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

7:g.30969116G>T
ENST00000326139.4:c.214G>T
ENSP00000320180.2:p.Glu72Ter

Variation displays