Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.46 (C)
Location

Chromosome 5:135377349 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60080137, rs56429354

This variation has 6 HGVS names - click the plus to show

5:g.135377349C>A
ENST00000504185.1:n.302-2398C>A
ENST00000506699.1:n.299-2398C>A
ENST00000442011.2:c.234-2398C>A
ENST00000507018.1:c.151-2398C>A
ENST00000305126.8:c.234-2398C>A

This variation has assays on 10 chips - click the plus to show

Variation displays