Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.34 (G)
Location

Chromosome 5:159315942 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR025273

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17875322, rs57107704

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

5:g.159315942T>G
ENST00000521472.3:n.289+4528T>G
ENST00000231228.2:c.*159A>C
LRG_71:g.19532A>C
LRG_71t1:c.*159A>C

This variation has assays on 5 chips - click the plus to show

Variation displays