Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 4:146636920 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60960355

HGVS name

4:g.146636920A>G

About this variant

This variant overlaps 3 transcripts and has 2513 individual genotypes.

Variation displays