Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.22 (C)
Location

Chromosome 4:155211295 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60721603

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

About this variant

This variant overlaps 5 transcripts, has 1168 individual genotypes and is mentioned in 1 citation.

Variation displays