Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 5:136041660 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60080137, rs56429354

This variation has 5 HGVS names - click the plus to show

5:g.136041660C>A
ENST00000506699.4:n.299-2398C>A
ENST00000504185.4:n.302-2398C>A
ENST00000442011.5:c.234-2398C>A
ENST00000507018.4:c.151-2398C>A

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 4543 individual genotypes and is mentioned in 1 citation.

Variation displays