Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 6:80626460 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM045143

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_045_ELOVL4_605512_0004, 13233

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

6:g.80626460G>C
ENST00000369816.4:c.810C>G
ENSP00000358831.4:p.Tyr270Ter

Variation displays